CClinicalTrials.gg
Status unknownNCT02279472Updated Oct 31, 2014

Optical Coherence Tomography Quantitative Analysis of Changes in Anterior Chamber After Laser Peripheral Lridotomy

An interventional study of Laserex Tango Nd:YAG, Ellex-SuperQ Medical, Australia in Primary Angle Closure Glaucoma, sponsored by Second Xiangya Hospital of Central South University. Status unknown at 1 site in China. Open to participants aged 30 Years to 80 Years. Per ClinicalTrials.gov, last updated 2014-10-31.

Sponsored by Second Xiangya Hospital of Central South University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Oct 2014), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Not applicable
Ages
30 Years to 80 Years
Sex
All
01

Study summary

The purpose of this study is to analysis changes in anterior segment morphology after laser peripheral lrldotomy measured by optical coherence tomography, and to evaluate treatment effectiveness

Read the detailed description

In the study ,primary angle closure(PAC) and primary angle closure glaucoma (PACG) will be recruited. Anterior segment optical coherence tomography images captured before and after laser peripheral iridotomy will be analysed to provide objective and reproducible quantification of anterior segment biometric parameters.The outcomes can provide useful information for clinical strategies in the treatment and management of pathology related to angle closure.

02

Conditions studied

  • Primary Angle Closure Glaucoma
03

In context

Glaucoma, Angle-Closure

95 studies on the registry are indexed under Glaucoma, Angle-Closure; 17 are open to participants now.

This study's planned enrollment of 40 is below the median of 57 across 59 interventional studies indexed under Glaucoma, Angle-Closure.

Browse Glaucoma, Angle-Closure studies →

Lead sponsor

Second Xiangya Hospital of Central South University is the lead sponsor of 82 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

1 .The gonioscopy or UBM examination has confirmed the diagnosis of PACS or PAC 2. Intraocular pressure within 10 to 21 mmHg ,C/D≤0.6 3. Visual field is normal or only show paracentral scotoma 4. Vision or corrected visual acuity ≥0.8 5. Refractive degree no more than 200D 6. Exclude other ocular and systemic diseases

Exclusion criteria

-

Exclusion Criteria:

  1. Corneal macula and other corneal diseases, ocular surface disease or corneal edema
  2. Iridocyclitis
  3. Ocular trauma and intraocular operation history
  4. No fixationFundus lesions such as diabetic retinopathy or retinal detachment
  5. No fixation
  6. Ocular or systemic application of cortical steroids -
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Other
    laser peripheral iridotomy

    Laser peripheral iridotomy (LPI) is widely regarded as the first-line intervention for either acute or chronic types of angle-closure glaucoma in early stage ,which relieves pupil block and thus flattening the iris contour and widening the drainage angle,performd by Nd.YAG LASER

    Procedure: Laserex Tango Nd:YAG, Ellex-SuperQ Medical, Australia

Interventions

  • ProcedureLaserex Tango Nd:YAG, Ellex-SuperQ Medical, Australia

    All the patients will be achieved with pilocarpine 1% for pupil constriction, laser peripheral iridotomy(LPI) is performed using the ophthalmic neodymium: yttrium aluminium garnet laser (Laserex Tango Nd:YAG, Ellex-SuperQ Medical, Australia) and an VOLK iridotomy contact lens. After LPI, patients will be given topical prednisolone acetate 0.1% for 7 days.

06

What researchers measure

Primary outcomes

  1. Changes in anterior chamber after LPI at 1 month

    Time frame: 1month

07

Study locations

1 of 1 sites recruiting
  • The Second Xiangya Hospital of Central South University,
    Changsha, Hunan 410000, China
    Recruiting
08

References and documents

Publications

  • Memarzadeh F, Li Y, Chopra V, Varma R, Francis BA, Huang D. Anterior segment optical coherence tomography for imaging the anterior chamber after laser peripheral iridotomy. Am J Ophthalmol. 2007 May;143(5):877-9. doi: 10.1016/j.ajo.2006.11.055. Epub 2006 Dec 29. PubMed 17452177 ↗
  • Lee KS, Sung KR, Shon K, Sun JH, Lee JR. Longitudinal changes in anterior segment parameters after laser peripheral iridotomy assessed by anterior segment optical coherence tomography. Invest Ophthalmol Vis Sci. 2013 May 3;54(5):3166-70. doi: 10.1167/iovs.13-11630. PubMed 23599331 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 31, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02279472
Lead sponsor
Second Xiangya Hospital of Central South University
Responsible party
Haomin Luo (Haomin Luo M.d., Second Xiangya Hospital of Central South University) — Principal investigator
First posted
Oct 31, 2014
Start date
Oct 2014
Primary completion
Dec 2014 (estimated)
Completion
Jan 2015 (estimated)
Last update
Oct 31, 2014

Study contacts

Haomin Luo, Ph.D student
Contact
lhmqqpp@163.com
+86 13875830738
Xuanchu Duan, Ph.D
study director · Central South University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2014. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion