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Glaucoma valve implantation with tube Insertion through Pars plans in neovascular glaucoma eyes

Glaucoma valve implantation with tube Insertion through Pars plans in neovascular glaucoma eyes

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-17010710
Enrollment
Unknown
Registered
2017-02-23
Start date
2017-03-01
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

experimental group:The experimental valve inserted

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 years; 2. The subjects had clinical manifestations of neovascular glaucoma; 3. The researchers determine need to use valves implanted the operation way of subjects; 4. Participants can't anterior chamber implantation valve: Anterior chamber depth< 2 mm; anterior chamber around the narrow corner < 1/2 CT; 5. The participants or their legal representatives to understand the research purpose, according to the research plan enough compliance, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. There are eyes neovascular glaucoma, and treatment of the subjects at the same time;Acute infectious eye disease subjects; Eye malignant tumor of the subjects; 2. There are serious refractive stromal opacity and may affect the operation of the subjects; 3. There are important viscera function failure or other serious disease, including clinical related coronary artery disease, Cardiovascular disease or myocardial infarction into the group of the first six months; Serious neurological or psychiatric illness; Serious infections; Coagulant function abnormality; There general active infectious diseases; 4. The subject participate in drug test or other medical instrument clinical trial subjects before 1 months; 5. Patients with mental illness to interfere with treatment and assessment; 6. Breastfeeding women or pregnant women; 7. 3 months prior to screening to participate in any clinical study or researchers think not suitable to participate in this clinical trial subjects.

Design outcomes

Primary

MeasureTime frame
intraocular pressure;

Secondary

MeasureTime frame
new vessels;

Countries

China

Contacts

Public ContactAo Rong

Shanghai Tongji Hospital

rongao@163.com+86 13818295715

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026