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A randomized controlled study of trabeculectomy combined with anterior chamber proliferative membrane interception and trabeculectomy alone in the treatment of neovascular glaucoma

A randomized controlled study of trabeculectomy combined with anterior chamber proliferative membrane interception and trabeculectomy alone in the treatment of neovascular glaucoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055138
Enrollment
Unknown
Registered
2022-01-01
Start date
2022-04-11
Completion date
Unknown
Last updated
2023-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

neovascular glaucoma

Interventions

Experimental group:Trabeculectomy combined with anterior chamber proliferative membrane interception

Sponsors

Affiliated Eye Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Sign the informed consent form and be willing to follow up according to the time specified in the trial; 2. Aged 18 to 75 years, gender is not limited; 3. Patients with neovascular glaucoma diagnosed with neovascularization on the surface of the iris and (or) the angle of the chamber; 4. The intraocular pressure is still greater than 22mmHg (1mmHg=0.133kPa) under the maximum intraocular pressure lowering drug.

Exclusion criteria

Exclusion criteria: 1. Neovascular glaucoma secondary to intraocular tumor or inflammation; 2. Severe cardiovascular and cerebrovascular diseases or recent active eye inflammation; 3. History of eye surgery such as cyclocondensation, scleral cerclage, glaucoma trabeculectomy, aqueous drainage valve implantation, and intravitreal silicone oil filling; 4. Patients who are planning to become pregnant, pregnant or breastfeeding; 5. Patients who have uncontrolled systemic diseases or other reasons and are judged by the investigator to be unsuitable to enter this study.

Design outcomes

Primary

MeasureTime frame
Intraocular pressure;Best-corrected vision acuity;Corneal endothelial cell count;

Secondary

MeasureTime frame
Visual field;

Countries

China

Contacts

Public ContactLiang Yuanbo

Affiliated Eye Hospital of Wenzhou Medical University

yuanboliang@126.com+86 577 8805 3506

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026