An interventional study of RayOne EMV Toric IOL and RayOne Monofocal IOL in Cataract and Corneal Astigmatism, sponsored by Rayner Intraocular Lenses Limited. Completed at 9 sites in United States. Open to participants aged 22 Years and older. Per ClinicalTrials.gov, last updated 2026-01-21.
Sponsored by Rayner Intraocular Lenses Limited · Not applicable, Interventional, and Treatment
The objectives of the clinical investigation are to determine the safety and performance of the RayOne EMV Toric (Model RAO210T) following unilateral implantation and approximately 6 months (120 to 180 days) of post-operative assessment, as a randomized comparison to aspheric monofocal control for low cylinder (1.50 D). This patient population with cataracts and low corneal cylinder (+1.00 to +1.50 D) will have the natural crystalline lens removed and replaced with an intraocular lens in the capsular bag.
This study is a prospective, multicenter, randomized, active controlled, masked (assessor and subject) pivotal investigation for unilateral implantation of low cylinder (1.50 D) toric IOL. It compares the Rayner RAO210T toric IOL to the Rayner RAO600C aspheric monofocal IOL. Subjects who sign the ICF are considered enrolled in the study. After signing the ICF, subjects will be screened for eligibility. Inclusion and Exclusion Criteria must be applied prior to subject randomization. Subjects who meet all protocol-specified eligibility criteria will be assigned to the randomized controlled study arms if the study eye's estimated IOL cylinder power using Barrett Toric Calculator is 1.50 D. Randomized subjects receive either the Rayner RAO210T Toric IOL (1.50 D low cylinder) or the Rayner RAO600C aspheric monofocal IOL in the study eye.
Up to 295 adult subjects will be enrolled (consented) assuming a 15% screen failure rate, then up to 250 subjects will be randomized, of which approximately 125 subjects will be randomized to receive low cylinder (1.50 D) RayOne EMV Toric (Model RAO210T) in one eye and approximately 125 subjects randomized to receive the RAO600C aspheric monofocal IOL in one eye, to complete 120-180 days follow-up for at least 100 subjects in each group.
All subjects who meet inclusion criteria will be assigned to the randomized controlled study arms to receive either the RAO210T toric IOL (1.50 D low cylinder) or the RAO600C aspheric monofocal IOL in the study eye according to a 1:1 ratio. Randomization will be stratified by site.
Up to 11 U.S. sites will be encouraged to enroll a minimum of 20 subjects. No site will enroll more than 25% of the subjects enrolled in the study.
If a subject has significant cataract in both eyes, it is recommended that cataract surgery is performed in one eye before the subject is enrolled in the study. Once a subject has been enrolled, it is recommended that the fellow eye does not undergo cataract surgery (except for a YAG capsulotomy) throughout the duration of the study. At screening, if both eyes qualify for the study, the eye to undergo cataract surgery and IOL implantation is the eye with worse pre-operative BCDVA. If pre-operative BCDVA is the same for each eye, the right eye will be the study eye.
Subjects will complete 6 study visits in approximately 9 months. Subject participation is calculated as the difference between the time of the pre-operative visit to completion of Visit 4 (120 to 180 days post-operative).
Standard clinical trial methods will be used to minimize bias, such as the use of site personnel performing manifest refraction and visual acuity assessments masked to subject treatment assignment, masking of subjects in the randomized controlled investigation evaluating low cylinder power, standardized test procedures, common Investigator training and common inclusion and exclusion criteria.
In order to minimize bias, measures will be taken to mask the site personnel performing post-operative manifest refraction and visual acuity assessments, as to the subject's treatment assignment until after the final database lock. Every attempt should be made to have the same masked site personnel perform the same masked post-operative assessments for an individual subject throughout the subject's study participation.
Subjects will be masked to their IOL assignment in the randomized controlled investigation evaluating low cylinder power. All material which may indicate the subjects' assignment, e.g., packaging, documents, etc., will be removed from any areas where subjects and/or masked site personnel may see them. Unmasked personnel will further be instructed to scrupulously avoid conversation and communication with masked personnel, subjects and all other persons regarding subjects' assignments, outcomes, clinical courses, and all other information potentially relevant to the study and its conduct.
Study Groups:
Sample Size Determination:
Subjects will be enrolled with the goal of completing a total of 200 subjects through Visit 4 within the randomized groups, of whom 100 were implanted with the low cylinder RayOne EMV Toric IOL (Model RAO210T) and 100 were implanted with the RAO600C monofocal IOL.
Effectiveness For effectiveness, 100 subjects (eyes) randomized to the Toric (test) group (lowest cylinder power +1.50D) and 100 subjects (eyes) randomized to the Monofocal (control) group completing Visit 4 yields over 98% statistical power to reject H0e in favor of H1e and conclude the Toric IOL has statistically significantly lower mean residual manifest cylinder at Visit 4 compared to the Monofocal IOL, using a one-sided t-test with an alpha level of 0.025 and assuming a true mean difference of 0.4 D and a standard deviation of 0.7 D in both groups.
Safety For safety, ISO 11979-7 and ANSI Z80.30 specifies that a minimum of 100 subjects should complete a clinical evaluation of an IOL, where a parent IOL has been approved, to obtain appropriate specificity around adverse event and visual acuity rates.
Handling of Missing Data:
Missing data will be imputed for selected endpoints using the methods specified under the analysis descriptions for the endpoints. Where possible, multiple imputation will be used. Except where mentioned in Section 7, missing data will not be imputed.
Multiplicity Considerations:
The overall type I error rate for the toric effectiveness analyses will be controlled at 0.05. The study will be considered successful if all of the primary effectiveness and safety endpoints are met. Thus, no adjustments for multiplicity are necessary.
All primary effectiveness and primary safety endpoints as described below are required to achieve successful outcomes in order to demonstrate study success.
1,629 studies on the registry are indexed under Cataract; 235 are open to participants now.
This study's enrollment of 274 is above the median of 79 across 1,092 interventional studies indexed under Cataract.
Browse Cataract studies →Rayner Intraocular Lenses Limited is the lead sponsor of 4 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Female subjects must be 1-year , surgically sterilized, or, if of , have a negative urine pregnancy test at the Pre-operative Visit. Women of childbearing potential must use an acceptable form of throughout the study.
Acceptable methods include at least one of the following: intrauterine (intrauterine device), hormonal (oral, injection, patch, implant, ring), barrier with spermicide (condom, diaphragm), or abstinence.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).
Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).
Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Postmenopausal
Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Childbearing potential
Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).
Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Contraception
Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.
Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Clinically significant
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
All subjects randomized to be implanted with the low cylinder (1.50 D) RayOne EMV Toric IOL (Model RAO210T)
Device: RayOne EMV Toric IOL · Procedure: Cataract Surgery
All subjects randomized to be implanted with the RAO600C Monofocal IOL
Device: RayOne Monofocal IOL · Procedure: Cataract Surgery
Implantation of intraocular lens.
Also known as: Model RAO210T
Implantation of intraocular lens.
Also known as: RAO600C
Removal of natural crystalline lens due to cataracts
Mean Magnitude of Residual Manifest Cylinder
Mean magnitude of residual manifest cylinder (as measured by manifest refractive cylinder).
Time frame: 120 to 180 days post-operatively
Adjusted Mean Difference Magnitude of Residual Manifest Cylinder
The adjusted mean difference of residual manifest cylinder (as measured by manifest refractive cylinder) between Toric and Monofocal groups will be given together with a 95% confidence interval and associated one-sided p-value. This endpoint will be considered successful if the one-sided p-value ≤ 0.025.
Time frame: 120 to 180 days post-operatively
Axis Misalignment (Frequency and Percentage 10 Degrees)
Frequency and percentage of RayOne EMV Toric (Model RAO210T) IOLs with IOL axis misalignment at Visit 4 (as determined by photographic method) less than 10 degrees.
Time frame: 120 to 180 days post-operatively
Axis Misalignment (Frequency and Percentage 20 Degrees)
Frequency and percentage of RayOne EMV Toric (Model RAO210T) IOLs with IOL axis misalignment at Visit 4 (as determined by photographic method) less than 20 degrees.
Time frame: 120 to 180 days post-operatively
Stability of Toric IOL Axis Orientation (Frequency and Percentage)
Stability of toric IOL axis orientation, expressed as frequency and percentage of RayOne EMV Toric (Model RAO210T) IOLs that rotate ≤ 5 degrees postoperatively between 30 to 60 days (Visit 3) and 120 to 180 days (Visit 4)
Time frame: 30 to 60 days and 120 to 180 days post-operatively
Rates of IOL Adverse Events Per ISO 11979-7
Rates of IOL adverse events through 120 to 180 days post-operatively (Visit 4) compared to the ISO Safety and Performance Endpoint (SPE) rates as described in ISO 11979-7. Rates of cumulative and persistent adverse events from ISO 11979-7 (2018) Table E.2 will be reported by treatment group (Toric test group, Monofocal control group) and AE type. Rates of adverse events will be compared to the SPE rate from Table E.2. The one-sided p-value from the exact binomial test of each hypothesis will also be provided for each adverse event. If none of these hypothesis test results are statistically significant, this endpoint will be considered successful for the toric IOL.
Time frame: 120 to 180 days post-operatively
Rates of All Other Adverse Events Not Included in ISO 11979-7
The eyes with at least one adverse event not included in the cumulative and persistent adverse events from ISO 11979-7 (2018) Table E.2 through 120 to 180 days post-operatively (Visit 4) will be presented by treatment group (Toric test group, Monofocal control group).
Time frame: 120 to 180 days post-operatively
Rates of Secondary Surgical Interventions for IOL Repositioning Due to IOL Misalignment
The percentage of eyes implanted with the Toric test group IOL requiring a secondary surgical intervention for IOL repositioning due to IOL misalignment through 120 to 180 days post-operatively (Visit 4), as well as a two-sided 95% exact binomial confidence interval for the percentage, will be presented.
Time frame: 120 to 180 days post-operatively
Rate of BCDVA of 0.30 logMAR or Better Compared to the ISO SPE Rates
The percentage of eyes that achieve a BCDVA at 4 meters of 0.30 logMAR or better at 120 to 180 days post-operatively (Visit 4) will be presented by treatment group (Toric test group, Monofocal control group) for the Safety Set and Best Case Set. If neither of these hypothesis test results are statistically significant, this endpoint will be considered successful for the toric IOL.
Time frame: 120 to 180 days post-operatively
Residual Manifest Cylinder Stratified by Preoperative Keratometric Cylinder
Residual manifest refractive cylinder by subgroups of 0.25 D preoperative keratometric cylinder at 120 to 180 days post-operatively
Time frame: 120 to 180 days post-operatively
Percent Change in Absolute Cylinder Stratified by Preoperative Keratometric Cylinder
Percent reduction in absolute cylinder (as measured by residual manifest cylinder / preoperative keratometric cylinder), at 120 to 180 days post-operatively. Positive numbers represent an decrease in cylinder and negative numbers represent an increase in cylinder.
Time frame: 120 to 180 days post-operatively
| Milestone | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Started | 118 | 120 |
| Completed | 117 | 116 |
| Not completed | 1 | 4 |
| Withdrew: Protocol violation | 1 | 0 |
| Withdrew: Withdrawal by subject | 0 | 2 |
| Withdrew: Subject was not implanted with the study device | 0 | 2 |
Mean magnitude of residual manifest cylinder (as measured by manifest refractive cylinder).
| Diopters | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Mean Magnitude of Residual Manifest Cylinder | -0.368 ± 0.334 | -0.780 ± 0.532 |
The adjusted mean difference of residual manifest cylinder (as measured by manifest refractive cylinder) between Toric and Monofocal groups will be given together with a 95% confidence interval and associated one-sided p-value. This endpoint will be considered successful if the one-sided p-value ≤ 0.025.
| Diopters | Combined Toric and Control Groups |
|---|---|
| Adjusted Mean Difference Magnitude of Residual Manifest Cylinder | -0.430 (-0.5441 to -0.3159) |
Frequency and percentage of RayOne EMV Toric (Model RAO210T) IOLs with IOL axis misalignment at Visit 4 (as determined by photographic method) less than 10 degrees.
| Participants | Toric (Test) Group |
|---|---|
| Axis Misalignment (Frequency and Percentage 10 Degrees) | 92 |
Frequency and percentage of RayOne EMV Toric (Model RAO210T) IOLs with IOL axis misalignment at Visit 4 (as determined by photographic method) less than 20 degrees.
| Participants | Toric (Test) Group |
|---|---|
| Axis Misalignment (Frequency and Percentage 20 Degrees) | 98 |
Stability of toric IOL axis orientation, expressed as frequency and percentage of RayOne EMV Toric (Model RAO210T) IOLs that rotate ≤ 5 degrees postoperatively between 30 to 60 days (Visit 3) and 120 to 180 days (Visit 4)
| Participants | Toric (Test) Group |
|---|---|
| Stability of Toric IOL Axis Orientation (Frequency and Percentage) | 100 |
Rates of IOL adverse events through 120 to 180 days post-operatively (Visit 4) compared to the ISO Safety and Performance Endpoint (SPE) rates as described in ISO 11979-7. Rates of cumulative and persistent adverse events from ISO 11979-7 (2018) Table E.2 will be reported by treatment group (Toric test group, Monofocal control group) and AE type. Rates of adverse events will be compared to the SPE rate from Table E.2. The one-sided p-value from the exact binomial test of each hypothesis will also be provided for each adverse event. If none of these hypothesis test results are statistically significant, this endpoint will be considered successful for the toric IOL.
| Participants | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Cumulative - Cystoid macular edema | 2 | 1 |
| Cumulative - Hypopyon | 0 | 0 |
| Cumulative - Endophthalmitis | 0 | 0 |
| Cumulative - Lens dislocation from posterior chamber | 0 | 0 |
| Cumulative - Mechanical pupillary block | 0 | 0 |
| Cumulative - Retinal detachment | 0 | 0 |
| Cumulative - Secondary Surgical Intervention | 2 | 0 |
| Persistent - Cornea Stroma Edema | 0 | 0 |
| Persistent - Cystoid macular edema | 0 | 0 |
| Persistent - Iritis | 0 | 0 |
| Persistent - Increased IOP | 0 | 0 |
The eyes with at least one adverse event not included in the cumulative and persistent adverse events from ISO 11979-7 (2018) Table E.2 through 120 to 180 days post-operatively (Visit 4) will be presented by treatment group (Toric test group, Monofocal control group).
| Participants | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Cornea Stroma Edema | 6 | 5 |
| Increased IOP | 4 | 7 |
| IOL decentration/malposition resulting in secondary surgical intervention | 1 | 0 |
| Iris pigment epithelium loss | 1 | 0 |
| Progression or onset diabetic retinopathy | 1 | 0 |
| Retained lens material | 1 | 0 |
| Secondary Surgical Intervention - Wound burp (aqueous tap, or paracentesis) | 1 | 0 |
| Other - Posterior capsular opacification requiring YAG capsulotomy | 14 | 4 |
| Other - Posterior vitreous detachment | 7 | 11 |
| Other - Corneal edema | 7 | 7 |
| Other - Anterior chamber cells greater than Grade 2 at Visit 1 | 5 | 1 |
| Other - Corneal abrasion | 3 | 0 |
| Other - Epithelial defect | 2 | 1 |
| Other - Choroidal nevus | 1 | 1 |
| Other - Corneal dellen | 1 | 1 |
| Other - Dermatochalasis | 1 | 1 |
| Other - Epiretinal membrane | 2 | 0 |
| Other - Subconjunctival hemorrhage | 1 | 1 |
| Other - Worsening dry eye disease | 1 | 1 |
| Other - Central capsular wrinkle | 1 | 0 |
| Other - Chemosis | 1 | 0 |
| Other - Double vision secondary to neurological adjustment following cataract surgery | 1 | 0 |
| Other - Epithelial basement membrane dystrophy | 1 | 0 |
| Other - Intraretinal hemorrhage | 1 | 0 |
| Other - Photophobia | 1 | 0 |
| Other - Retinal pigment epithelial mottling | 1 | 0 |
| Other - Superficial punctate keratitis | 1 | 0 |
| Other - Trace punctate epithelial erosions | 1 | 0 |
| Other - Visually significant corneal edema resulting in BCDVA of 0.3 or worse | 1 | 0 |
| Other - Worsening punctate epithelial erosion | 1 | 0 |
| Other - Conjunctival injection | 0 | 2 |
| Other - Dry eye disease | 0 | 1 |
| Other - Iritis | 0 | 1 |
| Other - Keratoconjunctivitis Sicca, not specified as Sjogrens | 0 | 1 |
| Other - Retinal pigment epithelial changes | 0 | 1 |
The percentage of eyes implanted with the Toric test group IOL requiring a secondary surgical intervention for IOL repositioning due to IOL misalignment through 120 to 180 days post-operatively (Visit 4), as well as a two-sided 95% exact binomial confidence interval for the percentage, will be presented.
| Participants | Toric (Test) Group |
|---|---|
| Rates of Secondary Surgical Interventions for IOL Repositioning Due to IOL Misalignment | 1 |
The percentage of eyes that achieve a BCDVA at 4 meters of 0.30 logMAR or better at 120 to 180 days post-operatively (Visit 4) will be presented by treatment group (Toric test group, Monofocal control group) for the Safety Set and Best Case Set. If neither of these hypothesis test results are statistically significant, this endpoint will be considered successful for the toric IOL.
| Participants | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Safety Set | 117 | 116 |
| Best Case Set | 112 | 111 |
Residual manifest refractive cylinder by subgroups of 0.25 D preoperative keratometric cylinder at 120 to 180 days post-operatively
| Diopters | Toric (Test) Group With Low Preoperative Keratometric Cylinder | Monofocal (Control) Group With Low Preoperative Keratometric Cylinder | Toric (Test) Group With High Preoperative Keratometric Cylinder | Monofocal (Control) Group With High Preoperative Keratometric Cylinder |
|---|---|---|---|---|
| Residual Manifest Cylinder Stratified by Preoperative Keratometric Cylinder | -0.413 ± 0.333 | -0.794 ± 0.535 | -0.286 ± 0.325 | -0.764 ± 0.533 |
Percent reduction in absolute cylinder (as measured by residual manifest cylinder / preoperative keratometric cylinder), at 120 to 180 days post-operatively. Positive numbers represent an decrease in cylinder and negative numbers represent an increase in cylinder.
| percent change | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Percent Change in Absolute Cylinder Stratified by Preoperative Keratometric Cylinder | 68.59 ± 29.17 | 36.11 ± 45.69 |
Collected over 6 months. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Toric (Test) Group | 0/117 (0%) | 1/117 (0.9%) | 49/117 (41.9%) |
| Monofocal (Control) Group | 0/116 (0%) | 0/116 (0%) | 40/116 (34.5%) |
| Event | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Secondary Surgical Intervention - Surgical removal of retained lens fragmentEye disorders | 1/117 | 0/116 |
| Event | Toric (Test) Group | Monofocal (Control) Group |
|---|---|---|
| Posterior capsular opacification requiring YAG capsulotomyEye disorders | 14/117 | 4/116 |
| Posterior vitreous detachmentEye disorders | 7/117 | 11/116 |
| Corneal edemaEye disorders | 7/117 | 7/116 |
| Increased IOPEye disorders | 4/117 | 7/116 |
| Cornea Stroma EdemaEye disorders | 6/117 | 5/116 |
| Anterior chamber cells greater than Grade 2 at Visit 1Eye disorders | 5/117 | 1/116 |
| Corneal abrasionEye disorders | 3/117 | 0/116 |
| Conjunctival injectionEye disorders | 0/117 | 2/116 |
| Cystoid macular edemaEye disorders | 2/117 | 1/116 |
| Epithelial defectEye disorders | 2/117 | 1/116 |
| Age, Categorical(Participants) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| <=18 years | 0 | 0 | 0 |
| Between 18 and 65 years | 36 | 23 | 59 |
| >=65 years | 82 | 97 | 179 |
| Age, Continuous(years) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| Mean | 67.7 ± 7.4 | 69.4 ± 7.0 | 68.5 ± 7.2 |
| Sex: Female, Male(Participants) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| Female | 66 | 70 | 136 |
| Male | 52 | 50 | 102 |
| Race/Ethnicity, Customized(Participants) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| American Indian or Alaska Native | 1 | 2 | 3 |
| Asian | 1 | 0 | 1 |
| Black or African American | 4 | 1 | 5 |
| Native Hawaiian or Other Pacific Islander | 0 | 0 | 0 |
| White | 112 | 115 | 227 |
| Multiple | 0 | 2 | 2 |
| Hispanic or Latino | 3 | 4 | 7 |
| Not Hispanic or Latino | 115 | 116 | 231 |
| Region of Enrollment(participants) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| United States | 118 | 120 | 238 |
| Study Eye(Participants) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| Right Eye (OD) | 62 | 73 | 135 |
| Left Eye (OS) | 56 | 47 | 103 |
| Axial Length(mm) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| Mean | 24.183 ± 1.118 | 24.120 ± 1.117 | 24.151 ± 1.116 |
| Anterior Chamber Depth(mm) | Toric (Test) Group | Monofocal (Control) Group | Total |
|---|---|---|---|
| Mean | 3.337 ± 0.401 | 3.247 ± 0.381 | 3.292 ± 0.393 |
15 further baseline measures are reported on the registry.
PDFs hosted by the registry, ClinicalTrials.gov.
Plan to share: Yes — all collected IPD will be made available to U.S. FDA for supporting premarket approval, all IPD that underlie results in a publication
Supporting information: Study protocol, Statistical analysis plan, Clinical study report
Time frame: 6 months after device approval in the US
Access criteria: To be determined by the study sponsor after device approval.
Ran from Aug 2023 to primary completion in Oct 2024, 14 months.
Results were first posted in Jan 2026, 1 year 2 months after primary completion.
Of 190 industry-sponsored interventional studies with no phase under Cataract, half reached primary completion within 16 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 28. This study's 14 months is below that.
Counting every sponsor, half of 490 studies reached it within 17 months; a quarter within 9 and three quarters within 28.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.
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Rayner Intraocular Lenses Limited