Pseudophakia clinical trials
The registry lists 54 studies for Pseudophakia across more than 10 countries. 8 are recruiting or about to start. 22 of them are mainly about Pseudophakia (how this is decided). Per ClinicalTrials.gov, last updated 2026-09-25.
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Who runs them
Medicontur Medical Engineering Ltd (4) · Eye Hospital Pristina Kosovo (4) · Berkeley Eye Center (4) · Medical University of Vienna (3) · Brighton and Sussex University Hospitals NHS Trust (3) · Vance Thompson Vision (2) · Toyos Clinic (2) · Vienna Hospital Association (2)
What is being tested here
Drugs under test in Pseudophakia studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 3
- Dec 2026Clinical Evaluation of Low Contrast Visual Performance and Low Light Phenomena in Patients With Various Intraocular Lens Implants · Dr. Daniel H. Chang, MD
- Jun 2027IOL Power Formula Prediction Accuracy at the Extremes of Axial Length: A Prospective Outcome Verification Study · Vienna Hospital Association
- Aug 2027IOL Position and Refractive Change After Nd:YAG Laser Posterior Capsulotomy · Vienna Hospital Association
Who these studies take
Of the 3 Pseudophakia studies recruiting now, 2 (67%) set no upper age limit and 0 (0%) stop at 75 or younger. 0 (0%) take children under 18. 0 (0%) are for women only and 0 (0%) for men only; 2 (67%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 0 (0%) | 0 (0%) |
| 18 | 0 (0%) | 0 (0%) |
| 30 | 2 (67%) | 2 (67%) |
| 40 | 3 (100%) | 3 (100%) |
| 50 | 3 (100%) | 3 (100%) |
| 65 | 3 (100%) | 3 (100%) |
| 75 | 3 (100%) | 3 (100%) |
| 85 | 2 (67%) | 2 (67%) |
Across all 54 studies, recruiting or not: 9% stop at 75 or younger and 6% at 65; 4% take children; 0% are for women only and 0% for men only; 33% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
How long Pseudophakia studies take
Of 16 observational studies under Pseudophakia, half reached primary completion within 10 months of starting, counting those still running.
| Start to primary completion | Every sponsor | Industry | Non-industry |
|---|---|---|---|
| Observational | 10 mo4–16 · 16 studies | — | — |
Each figure is the month by which half the studies had reached primary completion, with the range in which the middle half did. Studies still running count until their last registry update; studies that stopped early are left out. Phase 1 includes early phase 1; observational means prospective or not stated, as retrospective and cross-sectional studies date a window of data rather than a study. How these figures are worked out
Studies
Recruiting first, then most recently updated. Showing 50 of 54. Browse all 54 → or search them.
- Clinical Evaluation of Low Contrast Visual Performance and Low Light Phenomena in Patients With Various Intraocular Lens ImplantsRecruitingNCT072131671 country
- IOL Position and Refractive Change After Nd:YAG Laser Posterior CapsulotomyNot yet recruitingNCT078021451 country
- Treatment of Residual Myopic Refraction After 6 Months on Pseudophakic Patients Using Relex-SmileEnrolling by invitationNCT04693663Not applicable1 country
- Treatment of Residual Refraction Errors 6 Months After Trifocal IOL Implantation With Relex-SmileEnrolling by invitationNCT04712318Not applicable1 country
- IOL Power Formula Prediction Accuracy at the Extremes of Axial Length: A Prospective Outcome Verification StudyNot yet recruitingNCT077247951 country
- Safety and Efficacy of the Hydrophobic Intraocular Lens Asqelio Monofocal With Biaspheric DesignEnrolling by invitationNCT060561541 country
- Identification of Minimum Focal Points in Vision Curve FormationRecruitingNCT062608521 country
- Comparative Study of the Tomey OA-2000, Tomey CASIA2, and the LenStar LS900RecruitingNCT060650721 country
- Treatment of Residual Hypermetropic Refraction on Pseudophakic Patients Using Allogenic Fresh Myopic LenticuleActive, not recruitingNCT04692012Not applicable1 country
- Visual Outcomes After Extended Depth of Focus Intraocular Lens Implantation With and Without Digital AssistanceCompletedNCT064603891 country
- Visual Outcomes and Patient Satisfaction With Vivity IOL in Post Refractive PatientsCompletedNCT060649161 country
- Maximizing Visual Outcomes With Eyhance IOLsCompletedNCT056110731 country
- Visual Outcomes and Patient Satisfaction With Bilateral PanOptix Verses Bilateral SynergyCompletedNCT060411391 country
- Intermediate Vision in Patients With Clareon IOLs Compared to Eyhance IOLsCompletedNCT052268841 country
- Treatment of Macular Edema After Cataract Surgery with Subconjunctival AfliberceptTerminatedNCT03396861Phase 11 country
- Retrospective, Non-interventional Clinical Investigation of the Safety and Performance of 640AD Monofocal Intraocular LensCompletedNCT065789101 country
- Retrospective, Non-interventional, Comparative Clinical Investigation of the Safety and Performance of 690AD and 690ADY Monofocal Intraocular Lens Implantation With Extended Patient EnrolmentCompletedNCT065789231 country
- Clinical Outcomes of Patients Implanted With the RxSight Light Adjustable Lens (LAL)WithdrawnNCT064880661 country
- Clinical Investigation of the Safety and Performance of Model 690AD and Model 690ADY Monofocal Intraocular Lens ImplantationCompletedNCT057502251 country
- Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL)CompletedNCT045331911 country
- Synergy Lens Outcomes EvaluationCompletedNCT054181531 country
- Monofocal Extended Range of Vision (MERoV) StudyCompletedNCT040116961 country
- Evaluation of Visual Function After Bilateral Implantation of EDOF IOLsCompletedNCT05335408Not applicable1 country
- The Effects of Angle Kappa on Clinical Outcomes With the PanOptix Intraocular LensCompletedNCT042428751 country
- Retrospective Clinical Investigation of the Safety and Performance of 640PM Trifocal IOL Implantation in Patients With Cataract and/or Ametropia (Hyperopia, Myopia) and/or PresbyopiaCompletedNCT057359901 country
- Clinical Outcomes of an New EDOF IOL (Isopure®)CompletedNCT057046861 country
- Efficacy of Pilocarpine 1% in PresbyopiaStatus unknownNCT05578001Phase 31 country
- Comparison of Two Aspheric Intraocular Lenses for Micro-monovisionStatus unknownNCT05531110Not applicable1 country
- Toric Trifocal IOL Treatment With High Astigmatism and Hyperopia vs SMILE Enhancement After Trifocal IOL TreatmentCompletedNCT04468022Not applicable1 country
- Clinical Outcomes of Bromday (Bromfenac Ophthalmic Solution) 0.09% QD vs. Nevanac (Nepafenac Ophthalmic Suspension) 0.1%CompletedNCT01310127Phase 4
- Intermediate Vision in a Driving Simulator Environment: Comparison of the J&J EYHANCE With a Conventional Monofoc. IOLCompletedNCT040592891 country
- Subjective and Objective Refraction in Pseudophakic PatientsCompletedNCT04319497Not applicable1 country
- Correlation Between Sulcus Anatomy and Other Parameters After Horizontal & Vertical Intraocular Lens (IOLs) PlacementsCompletedNCT04208633Not applicable1 country
- Tecnis Eyhance Versus Rayner RayOne StudyStatus unknownNCT04175951Not applicable1 country
- Reading Quality in Three Different Patient GroupsStatus unknownNCT03751241Not applicable1 country
- Pilocarpine and Brimonidine in Patients With Monofocal LensesStatus unknownNCT03825081Early Phase 11 country
- Polarization Perception in Health and Disease. Testing a New Sight TestStatus unknownNCT038230921 country
- Clinical Outcomes and Evaluation of Lotemax 0.5% in Treatment of Ocular Inflammation Associated With Cataract SurgeryCompletedNCT013442261 country
- Long-term Intraocular Lens (IOL) Decentration and Tilt in Eyes With Pseudoexfoliation Syndrome (PES) Following Cataract SurgeryCompletedNCT03453827
- A Clinical Trial to Evaluate a Corneal Inlay for the Improvement of Near and Intermediate Vision in Pseudophakic Presbyopic SubjectsStatus unknownNCT02668523Phase 31 country
- Corrected VA With Long-Term Follow-Up After AcrySof® Intraocular Lens (IOL) ImplantationCompletedNCT02450799Not applicable
- Modification in Cortical Activation in Pseudophakic Patients With Visual Difficulties After a Multifocal ImplantationWithdrawnNCT02529098Not applicable1 country
- Presbyopic Supracor Treatment for Near Myopic/Hyperopic Pseudophakic EyesCompletedNCT01387360Phase 41 country
- Posterior Capsule Opacification and Frequency of Nd:YAG Treatment and of Two Microincision IOLs: Hoya iMics NY-60 vs Acrysof SN60WFCompletedNCT01732484Not applicable
- Posterior Capsule Opacification and Frequency of Nd:YAG Treatment and of Two Microincision IOLs: Tecnis ZCB00 and Acrysof SA60ATCompletedNCT01742910Not applicable1 country
- The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic PatientsCompletedNCT01280110Phase 41 country
- Randomized, Masked Comparison of Bromfenac and Besifloxacin BID With Either Prednisolone BID or Loteprednol 0.5% BID for Prevention of Retinal Thickening and CME Following PhacoemulsificationStatus unknownNCT01193504Phase 41 country
- Effect of Posterior Corneal Toricity on Refractive Outcome of PseudophakiaStatus unknownNCT01554761Phase 41 country
- An Open-Label Evaluation of Degree of Accommodation in Pseudophakic Patients Bilaterally Implanted With Monofocal Intraocular LensesCompletedNCT010045491 country
- Analysis of the Effect of Intravitreal Dexamethasone Injection on Diabetic Macular Edema After Cataract Surgery (IDDMECS)CompletedNCT01030601Phase 21 country