Intravitreal Bevacizumab for Proliferative Diabetic Retinopathy

Sponsor
Khon Kaen University
Study ID
NCT01724385
Phase
PHASE4
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
20 Years - 60 Years
Healthy Volunteers
Not accepted

Interventions

Study Details

To evaluate the efficacy of intravitreal bevacizumab injections for treatment of proliferative diabetic retinopathy (PDR) with new dense vitreous hemorrhage (VH) after previous full panretinal photocoagulation (PRP).

Key Dates

First listed
Nov 9, 2012
Start date
Aug 31, 2012
Status verified
Apr 2013
Primary completion
Dec 31, 2012
Completion
Dec 31, 2012

Study Design

Enrollment
18 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: intravitreal bevacizumab injection
    intravitreal injection of bevacizumab 1.25 mg

Primary Outcome Measure

The percentage of eyes that vitreous hemorrhage has been completely resolved [ Time Frame: 12 months ]