MedPath

Evaluation of Intravitreal injection of Bevacizumab for treatment of Chronic Central Serous Chorioretinopathy

Not Applicable
Conditions
chronic central serous chorioretinopathy.
Disease of the eye and adnexa
Registration Number
IRCT201202198983N1
Lead Sponsor
Guilan Universoty of Medical Sciences, Pro-vice-chancellor for resea
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
15
Inclusion Criteria

Inclusion criteria :
1- patient by Acute Central Serous Chorioretinopathy for more than 4-months.
2- Comformation of The Chronic Central Serous Chorioretinopathy byOcular Coherent Tomography(OCT) and Fluorescien Angiography (FFA) .
3- comfirmation of the Diseasis by Supervisor of Study.

Exclusion criteria:
1- Chronic Central Serous Chorioretinopathy more than 2 years.
2- History of Treatment by any type of Laser.
3-History of Thromboambolic Diseasis Like Myocardial Infarction and Cerebro Vascular accident.
4- History of Treatment by Intravitreal Avastin during 2 months ago.
5- any sistemic Diseasis that need Oral Corticosteroid Thrapy.
6- un - Controled Glaucoma
7- Pregnancy
8- Lack of agreement by Patient for periodic Follow up during study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Vision Improvement. Timepoint: every 6 to 8 weeks untill 6 month. Method of measurement: Snelen Chart.;Anatomical Improvement. Timepoint: every 6 to 8 weeks untill 6 month. Method of measurement: Clinical exam and OCT.
Secondary Outcome Measures
NameTimeMethod
Centeral thickness of retin. Timepoint: per 6-8 weeks till 6 month. Method of measurement: with OCT.If in the first examination( by OCT) after weeks 6 to 8 ,at least 10 % reduction in the central macular thickness occur,the patient will be periodically follow,if not ,the patient will be omitted.
© Copyright 2025. All Rights Reserved by MedPath