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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202198983N1
Enrollment
15
Registered
2012-03-17
Start date
2012-02-19
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

chronic central serous chorioretinopathy. Disease of the eye and adnexa

Interventions

In the operating room, under local anesthesia, and MAC and sterile condition by using 10% & 5% Betadine for periorbital and culdesac area and prep & drape and insertion of speculum and after 0.1 c
Treatment - Drugs

Sponsors

Guilan Universoty of Medical Sciences, Pro-vice-chancellor for resea
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Rasoul Sabouri

Guilan university of Medical Sciences

sabouri@gums.ac.ir+98 13 1223 6886

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026