CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 22 enrolled
Drug / intervention
intravitreal injection of ranibizumab +3 moredrug
Likely dose
intravitreal injection of ranibizumab 0.5 mgfrom 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/NCT00815360
NCT00815360Phase 2Completed

Ranibizumab (rhuFab V2) and Scatter Laser Photocoagulation in Treatment of Patients With Clinically-significant Diabetic Macular Edema With Peripheral Retinal Nonperfusion (RaScaL)

Retina Associates of Florida, P.A.·interventional·Posted Dec 30, 2008·Updated Mar 5, 2015

In Brief

A Phase 2 clinical trial evaluating intravitreal injection of ranibizumab, peripheral laser, and 2 other interventions for Diabetic Macular Edema. Completed, enrolled 22 participants across 1 site.

Detailed Summary

To investigate the role of ranibizumab and angiographically-directed peripheral scatter laser therapy in patients with clinically-significant diabetic macular edema (CSME) and peripheral nonperfusion. We propose a novel treatment of CSME in a subgroup of patients defined by a combination of ultrawide-field angiography (UWFA) and optical coherence tomography (OCT). Within this classification scheme, patients with CSME are subdivided by the presence of: 1) focal macular leakage, 2) vitreomacular interface traction, and/or 3) peripheral nonperfusion. The successful treatment of diabetic macular edema would be dictated by pathophysiology-directed therapy based on this classification. The subgroup of interest for this clinical trial is characterized by diabetic macular edema, peripheral nonperfusion on UWFA, and the absence of macular traction on OCT. This group of patients has previously not been well recognized or characterized due to limitations in previous, standard angiographic evaluation of the retinal periphery. We postulate that this subcategory represents one with a high rate of failure of accepted therapies given persistence of the basic pathophysiologic mechanism for CSME, namely ischemia-induced production of Vascular Endothelial Growth Factor (VEGF) from the retinal periphery. This also represents a population of patients with likely recurrence of CSME despite treatment with anti-VEGF therapy alone for the same reason.

Study Details

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

Timeline

Phase 2CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 30, 2008
Enrollment StartFeb 1, 2008
Primary CompletionJul 1, 2011
Study CompletionAug 1, 2011
TodayJul 2, 2026
Enrollment to primary: 3.4 yearsPosted 17.5 years ago

Interventions

intravitreal injection of ranibizumabdrug

intravitreal injection of 0.5 mg ranibizumab

peripheral laserprocedure

ultra-widefield fluorescein angiography guided peripheral laser

intravitreal injection of triamcinolone acetonidedrug

intravitreal injection of 4.0 mg triamcinolone acetonide

macular laserprocedure

macular laser to areas of retinal thickening or leakage