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Clinical Trials/NCT01051583
NCT01051583CompletedPhase 2

Avastin as an Adjunct to Diode Laser Cyclophotoablation in the Treatment of Neovascular Glaucoma

Cairo University1 site in 1 country16 target enrollmentStarted: January 1, 2006Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
16
Locations
1
Primary Endpoint
Disappearance of iris neovessels

Study Overview

Brief Summary

Assess the efficacy of Avastin as an adjunct to Diode Laser cyclophotocoagulation in the treatment of Neovascular Glaucoma.

Detailed Description

Design: Prospective, comparative interventional case series. Method: Patients were randomly assigned into Group A which were treated with Diode laser cyclophotocoagulation alone, whereas group B received intravitreal Avastin (One milligram = 0.04mL of 25 mg/mL) in conjunction with the Diode Laser. The preoperative data included etiology, mean age; follow up period, and a full ophthalmological examination with emphasis on mean IOP, iris neovascularization, pain and corneal edema.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
14 Years to 72 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Neovascular absolute glaucoma
  • •Painful blind eyes

Exclusion Criteria

  • •Neovascular glaucoma with useful vision or potential for useful vision

Arms & Interventions

Avastin , diode laser cyclophotcoagulation

Experimental

Intravitreal Avastin injection in conjunction with diode laser cyclophotocoagulation

Intervention: Diode laser cyclophotocoagulation enhanced by intravitreal injection of Avastin (Procedure)

Diode Laser cyclophotocoagulation

Active Comparator

Diode laser cyclophotocoagulation to control intraocular pressure

Intervention: Diode laser cyclophotocoagulation enhanced by intravitreal injection of Avastin (Procedure)

Outcomes

Primary Outcomes

Disappearance of iris neovessels

Time Frame: 2 weeks

Secondary Outcomes

  • Intra ocular pressure(4 weeks)

Investigators

Sponsor Class
Other

Study Sites (1)

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