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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00370669
Other study ID # 8411
Secondary ID
Status Recruiting
Phase Phase 3
First received August 30, 2006
Last updated February 21, 2007
Start date November 2005
Est. completion date February 2007

Study information

Verified date February 2007
Source hahid Beheshti University of Medical Sciences
Contact Masoud Soheilian, MD
Phone +98 21 22585952
Email labbafi@hotmail.com
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

to compare the effect of intravitreal bevacizumab alone or in combination with triamcinolone acetonide with laser photocoagulation on clinically significant macular edema (CSME)


Description:

we entered 150 eyes into the study that recruitment of cases finished recently.Eligible eyes randomly assign to one of the study arms including intravitreal bevacizumzb, intravitreal bevacizumzb/triamcinolone and macular photocoagulation groups. Every patient needs at least 1 year followup. During this time BCVA, OCT, FA will be done for each patient and inaccording to interpretation of datas and fundus exam repeatation of injection will be done.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date February 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- case with clear media IOP below 23 mm/Hg female after menopause at least for 12 months or had 2 contraceptive roots visual acuity between 20/50 to 20/320

Exclusion Criteria:

- no PRP or N.d YAG laser in past 6 months no intraocular surgery in past 12 months

- CVA in past 12 months blood sugar above 250

- active infection in extraocular adnexa

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:
bevacizumab

triamcinolone acetonide


Locations

Country Name City State
Iran, Islamic Republic of Masoud Soheilian 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
Primary central macular thickness
Secondary Leakage in fluorescein angiography
Secondary intraocular pressure
Secondary cataract progression
Secondary anterior chamber reaction
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