CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 75 enrolled
Drug / intervention
Avastin® (bevacizumab) +1 moredrug
Likely dose
Avastin® (bevacizumab) 0.1 mLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01996826
NCT01996826Phase 2Completed

A Multi-Center Study of the Safety and Efficacy of Bevacizumab in High-Risk Corneal Transplant Survival

Reza Dana, MD·interventional·Posted Nov 27, 2013·Updated Aug 10, 2020

In Brief

A Phase 2 clinical trial evaluating Avastin® (bevacizumab) and 0.9% NaCl & Refresh Liquigel for Corneal Neovascularization and Corneal Graft Failure. Completed, enrolled 75 participants across 3 sites.

Detailed Summary

The goal of this study is to investigate whether using bevacizumab (Avastin®) is both safe and effective at decreasing the likelihood of a high-risk corneal graft rejection. Patients who are "high-risk" for rejection have blood vessels growing from the white of the eye into the cornea (clear, front region of the eye). The medication is used at the time of surgery and in the weeks following surgery. Participants have a 50/50 chance at receiving the active study medication or a placebo medication.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedNov 27, 2013
Enrollment StartApr 1, 2014
Primary CompletionApr 1, 2019
TodayJul 2, 2026
Enrollment to primary: 5 yearsPosted 12.6 years ago

Interventions

Avastin® (bevacizumab)drug

One time subconjunctival injection of 0.1 mL (2.5 mg) bevacizumab followed by topical treatment with 1% solution bevacizumab four times a day for four weeks.

0.9% NaCl & Refresh Liquigeldrug

One-time subconjunctival injection of 0.1mL 0.9% NaCl followed by topical treatment with Refresh Liquigel four times a day for four weeks.