Clinical Trials Directory

Trials / Unknown

UnknownNCT01151722

Adjuvant Intravitreal Bevacizumab in Pars Plana Vitrectomy for Diabetic Vitreous Hemorrhage

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
2 (estimated)
Sponsor
University of Sao Paulo · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Postoperative vitreous hemorrhage is a common complication after vitrectomy for proliferative diabetic retinopathy. There have been efforts to lower the incidence of postoperative vitreous hemorrhage such as preoperative bevacizumab injection. Bevacizumab (Avastin) is a potent inhibitor of angiogenesis and has been shown to decrease retinal and iris neovascularization in proliferative diabetic retinopathy. Recently there have been reports showing that preoperative bevacizumab injection could reduce intraoperative bleeding from abnormal vessels and could make surgery easier and more successful. Our hypothesis is that intraoperative bevacizumab injection could reduce postoperative vitreous hemorrhage by inhibiting the vessel formation after surgery. We started the prospective randomized comparative study to determine the effect of pre and intra-operative bevacizumab injection on postoperative vitreous hemorrhage after diabetic vitrectomy in comparison to vitrectomy without any adjuvant drug.

Conditions

Interventions

TypeNameDescription
PROCEDUREbevacizumab injectionbevacizumab injection before vitrectomy
PROCEDUREbevacizumab injectionbevacizumab injection after vitrectomy

Timeline

Start date
2009-12-01
Primary completion
2010-12-01
First posted
2010-06-28
Last updated
2010-06-28

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01151722. Inclusion in this directory is not an endorsement.