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Ranibizumab in the treatment of neovascular glaucoma

Ranibizumab in the treatment of neovascular glaucoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-14005709
Enrollment
Unknown
Registered
2014-12-01
Start date
2012-12-25
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

neovascular glaucoma

Interventions

Injection group:Intravitreal Ranibizumab 0.5 mg / 0.05 ml
Control:Without intravitreal Ranibizumab

Sponsors

Shanghai First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. neovascular glaucoma patients with age between 18 and 85 years old; 2. intraocular pressure higher than 22 mm Hg (1 mm Hg = 0.133 kPa, Goldmann applanation tonometry) with additional anti-glaucoma medicines; 3. with or without intravitreal Ranibizumab 0.5 mg/0.05 ml from 1 to 5 days before Ahmed glaucoma valve implantation; 4. to finish at least 6 months follow-up.

Exclusion criteria

Exclusion criteria: 1. with other type of glaucoma or other serious ocular disease; 2. previous anti-glaucoma surgery or other intraocular surgery; 3. previous intravitreal injection within 3 months; 4. less than 6 months follow-up; 5. difficult to measure intraocular pressure; 6. combined with cataract surgery or vitreal surgery; 7. binocular surgery or intravitreal injection; 8. pregnant or with uncontrolled internal medicine disease.

Design outcomes

Primary

MeasureTime frame
intraocular pressure;surgical success rate;best corrected visual acuity;

Secondary

MeasureTime frame
additional anti-glaucoma medicine;operative complications;

Countries

China

Contacts

Public ContactTang Min
tmsmile@sina.com+86 13817700414

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026