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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00370539
Other study ID # 8542
Secondary ID
Status Recruiting
Phase Phase 3
First received August 30, 2006
Last updated November 13, 2006
Start date September 2006
Est. completion date November 2006

Study information

Verified date November 2006
Source hahid Beheshti University of Medical Sciences
Contact Hamid Ahmadieh, MD
Phone +98 21 22585952
Email hahmadieh@hotmail.com
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

To compare the efficacy and safety of photodynamic therapy (PDT) combined with intravitreal bevacizumab versus combination of photodynamic therapy , intravitreal bevacizumab and intravitreal triamcinolone for neovascular AMD.


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date November 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility Inclusion Criteria:

- Cases of active neovascular AMD with visual acuity of 20/400- 20/40

Exclusion Criteria:

- History of glaucoma or ocular hypertension

- Disciform scar

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
verteporfin, bevacizumab, triamcinolone acetonide


Locations

Country Name City State
Iran, Islamic Republic of Hamid Ahmadieh, MD 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 Visual acuity
Secondary Central macular thickness
Secondary Leakage in fluorescein angiography
Secondary Intraocular pressure
Secondary Anterior chamber reaction
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