Skip to content

Effect of Intravitreal Bevacizumab on Clinically Significant Macular Edema

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00370669
Enrollment
150
Registered
2006-09-01
Start date
2005-11-30
Completion date
2007-02-28
Last updated
2007-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Macular Edema

Keywords

Bevacizumab, CSME, MPC, Triamcinolone acetonide

Brief summary

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

Detailed 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.

Interventions

DRUGbevacizumab
DRUGtriamcinolone acetonide

Sponsors

Shahid Beheshti University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
visual acuity
central macular thickness

Secondary

MeasureTime frame
Leakage in fluorescein angiography
intraocular pressure
cataract progression
anterior chamber reaction

Countries

Iran

Contacts

Primary ContactMasoud Soheilian, MD
labbafi@hotmail.com+98 21 22585952

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026