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Minimally Invasive Suprachoroidal Drainage for the Treatment of Neovascular Glaucoma

An Exploratory Study of the Efficacy and Safety of Minimally Invasive Supraporoidal Drainage for Advanced Neovascular Glaucoma

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07201415
Enrollment
30
Registered
2025-10-01
Start date
2025-01-01
Completion date
2027-03-01
Last updated
2025-10-01

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

Conditions

Neovascular Glaucoma

Keywords

Neovascular glaucoma, Retinal Vein Occlusion, Diabetic Retinopathy, Treatment

Brief summary

To explore the efficacy and safety of minimally invasive suprachoroidal drainage for the treatment of advanced neovascular glaucoma

Detailed description

To explore the efficacy and safety of minimally invasive supraporcular drainage in the treatment of advanced neovascular glaucoma, and to record the various basic diseases, ocular conditions, lifestyle, inflammatory markers and other parameters of NVG patients. To compare the safety and efficacy of new surgical methods and traditional surgical methods in order to find an effective treatment for neovascular glaucoma

Interventions

PROCEDUREminimally invasive suprachoroidal drainage

minimally invasive suprachoroidal drainage

Sponsors

Zhongnan Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Advanced (angle-closure) neovascular glaucoma with poorly controlled intraocular pressure (IOP \> 21mmHg) after medical or surgical treatment

Exclusion criteria

* Various other types of glaucoma (including primary open-angle glaucoma, primary open-closed glaucoma, normal tension glaucoma, juvenile glaucoma, congenital glaucoma, other special types of glaucoma, etc.) * Eye infection within two weeks before surgery * Non-glaucomatous intraocular diseases that affect intraocular pressure (choroidal hemorrhage or detachment, retinal detachment, lens subluxation, thyroid eye disease, clinically significant macular edema, eye tumors, etc.) * Visual acuity of non-study eyes \< 0.05 * Congenital or acquired factors lead to ciliary body anatomical abnormalities

Design outcomes

Primary

MeasureTime frameDescription
Ocular biological parameters1 day, 1 week, 1 month, 3 months, and 6 months after surgeryintraocular pressure
Surgical outcome measures1 day, 1 week, 1 month, 3 months, and 6 months after surgeryuse of intraocular pressure lowering drugs
The success rate of surgery was evaluated according to the specific value of intraocular pressure after surgery1 day, 1 week, 1 month, 3 months, and 6 months after surgeryComplete success was defined as IOP within the normal range with no drug dependence, conditional success was defined as IOP within the normal range with drug dependence, and failure was defined as the rest

Secondary

MeasureTime frameDescription
The effective rate of surgery was evaluated according to the amplitude of IOP reduction after surgery and the change in the number of IOP-lowering drugs1 day, 1 week, 1 month, 3 months, and 6 months after surgeryAmplitude of IOP reduction: IOP change/initial IOP.The total number of IOP lowering drugs was recorded based on the number of active ingredients
Surgical outcome measures1 day, 1 week, 1 month, 3 months, and 6 months after surgerycomplications

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026