Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01232179
Other study ID # 88100
Secondary ID
Status Recruiting
Phase Phase 2
First received November 1, 2010
Last updated November 1, 2010
Start date October 2010
Est. completion date May 2011

Study information

Verified date October 2010
Source hahid Beheshti University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics commitee
Study type Interventional

Clinical Trial Summary

Proliferative diabetic retinopathy (PDR) is treated with conventional pan retinal photocoagulation (PRP) which can improve the visual prognosis in this complication significantly. However , the treatment may also resulting adverse effects such as blurring of central vision, visual field constriction and disturbance in dark adaptation and contrast vision. Extended targeted retinal coagulation (TRP) to the ischemic areas may cause regression of the neovascularization while minimizing some of the risks and complication associated of treatment of PDR with these two methods.


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date May 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- patients with PDR condidate for photocoagulation teraphy

- Pupil with dilatasion=6mm

- without privious treatment with anti VEGF drugs 3months before study

- without privious vitroretinal sugery

- without privoius lasertraphy

Exclusion Criteria:

- To have NVI cricteria with increase of inraocular pressure

- to have cataract or vitrus leakage which prevent lasertraphy

- pupil smaller that 6mm

- traditional retinal detachment

- privious treatment with anti VEGF drugs 3months before study

- privious PRP

- patient unable to get wide field FAG

Study Design

Allocation: Randomized, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
conventional prp
pan retinal photocoagulation
targeted prp
1200-1600 spot in far periphery retin, anterior equator

Locations

Country Name City State
Iran, Islamic Republic of Labbafinejad medical center Tehran

Sponsors (1)

Lead Sponsor Collaborator
hahid Beheshti University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary no leakage in widefield fluorescin angiography 3 months after lasertraphy No