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The Effect of Therapy With Bevacizumab in Chronic Central Serous Chorioretinopathy

Intraocular Concentrations of Growth Factors and Cytokines in Chronic Central Serous Chorioretinopathy And the Effect of Therapy With Bevacizumab

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00864773
Enrollment
10
Registered
2009-03-19
Start date
2009-03-31
Completion date
2010-03-31
Last updated
2009-03-19

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

Conditions

Central Serous Chorioretinopathy

Brief summary

The pathophysiology of central serous chorioretinopathy remains controversial. traditional treatment is laser photocoagulation or photodynamic therapy.Recently Bevacizumab (Avastin, Genetech),an antibody to vascular endothelial growth factor (VEGF),has known antipermeability properties and therefore may theoretically reverse the changes seen in central serous chorioretinopathy. The aim of this study is To investigate concentrations of growth factors and inflammatory cytokines and to report the effect of therapy with bevacizumab in eyes with central serous chorioretinopathy

Interventions

PROCEDUREintravitreal injection with anterior paracentesis

0.1cc Aqueous humor samples were taken each time an intravitreal injection of bevacizumab (2.5 mg in 0.1 ml)

Sponsors

Hallym University Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patients with a diagnosis of central serous chorioretinopathy * Idiopathic neurosensory retinal elevation demonstrated by optical coherent tomography * Presence of focal leaks at the level of the RPE on fluorescein angiography

Exclusion criteria

* Known side effects of systemic bevacizumab administration * Have a significant cardiovascular or thromboembolic history or were pregnant

Design outcomes

Primary

MeasureTime frame
Concentrations of growth factors and inflammatory cytokines in Aqueous humorat baseline

Secondary

MeasureTime frame
Central macular thickness at optical coherence tomographybaseline, 1 month, 3 months, 6 months

Outcome results

None listed

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