Status:

ACTIVE_NOT_RECRUITING

KDR2-2 Suspension Eyedrop in the Treatment of Neovascular Glaucoma (KDR-NVG) Trial

Lead Sponsor:

Sun Yat-sen University

Conditions:

Neovascular Glaucoma

Neovascularization

Eligibility:

All Genders

18-75 years

Phase:

PHASE1

Brief Summary

The clinical trial is aimed to evaluate the anti-neovascular effect of KDR2-2 suspension eyedrop in the treatment of neovascular glaucoma. Fourty subjects would receive either 0.96 or 3.84 mg/per day/...

Detailed Description

Neovascular glaucoma (NVG) has a high blinding rate and poor prognosis. Anti-glaucoma surgery is the main stake of saving visual function and relieving pain, but the proliferation of iris neovasculari...

Eligibility Criteria

Inclusion

  • Age 18-75;
  • The best-corrected visual acuity (BCVA) of the included eyes was \<0.01 (Snellen chart);
  • The BCVA of the contralateral eye of the included subjects was \>0.1;
  • Patients with clinically diagnosed neovascular glaucoma; The diagnostic criteria for neovascularization glaucoma were as follows: Intraocular pressure \> 21mmHg measured by Goldmann applanation tonometer; Neovascularization is seen in the iris or anterior chamber angle, with or without corneal edema;
  • Compliance with follow up for more than 28 days and written informed consent obtained;

Exclusion

  • Intravitreal injection of anti-VEGF drugs within 3 month before enrollment;
  • Participation in other clinical trials within 1 month;
  • Suffering from other ocular diseases that affect ocular examinations (e.g. keratopathy, uveitis, intraocular infection, etc.);
  • Those who plan to receive ocular surgery during the follow-up period;
  • Premenopausal women without birth control;
  • Having other systemic diseases such as severe liver and kidney function damage, cardiovascular disorders, respiratory disorders, etc.) that may affect the anti-neovascular effect of KDR2-2 or more likely to develop adverse events ;
  • Systemic infections under treatment;
  • Any study in which the physician believes that the patient's condition will interfere with the clinical trial (e.g., the patient is prone to stress, mood disorders, depression, etc.);

Key Trial Info

Start Date :

April 19 2021

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2024

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT04844619

Start Date

April 19 2021

End Date

December 31 2024

Last Update

December 11 2024

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Zhongshan Ophthalmic Center

Guangzhou, Guangdong, China, 51000