Clinical Trials Directory

Trials / Completed

CompletedNCT00802126

Intravitreal Bevacizumab and Low Fluence Photodynamic Therapy

Efficacy of Combining Intravitreal Bevacizumab With Photodynamic Therapy Using Reduced Light Fluence Rate in Choroidal Neovascularization Secondary to Pathologic Myopia.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
University of Campania Luigi Vanvitelli · Academic / Other
Sex
All
Age
35 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to report the treatment effect and safety of combined intravitreal bevacizumab (IVB) and photodynamic therapy (PDT) with verteporfin using a reduced (RF) light fluence rate, in choroidal neovascularization (CNV) secondary to pathologic myopia.

Detailed description

In this retrospective interventional case series, 16 patients with myopic CNV were included. All patients were treated with 1.25 mg of intravitreal bevacizumab followed by RF-PDT (25 J/cm²), 2 days later. All patients were previously treated with IVB monotherapy and active leaking of CNV occurred 90 to 120 days after the treatment. Best-corrected visual acuity (BCVA-ETDRS), foveal thickness (FT) on optical coherence tomography (OCT), and fluorescein and indocyanine green angiographic (FA; ICG) findings were recorded. Follow-up evaluations were carried out for 12 months.

Conditions

Interventions

TypeNameDescription
DRUGCombination therapy "IVB + rf-PDT"low-fluence photodynamic therapy combined with intravitreal bevacizumab

Timeline

Start date
2007-11-01
Primary completion
2008-12-01
Completion
2009-05-01
First posted
2008-12-04
Last updated
2016-02-08

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT00802126. Inclusion in this directory is not an endorsement.