Bevacizumab Versus Micropulse in Central Serous Chorioretinopathy (CSC)
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ClinicalTrials.gov Identifier: NCT00802906 |
Recruitment Status :
Completed
First Posted : December 5, 2008
Last Update Posted : September 27, 2012
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Central Serous Chorioretinopathy | Device: subthreshold micropulselaser Drug: bevacizumab | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 12 participants |
Allocation: | Non-Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Prospective Study on the Efficacy of 1.5mg Bevacizumab Versus Selective Subthreshold Micropulslaser in Central Serous Chorioretinopathy |
Study Start Date : | May 2007 |
Actual Primary Completion Date : | November 2010 |
Actual Study Completion Date : | December 2010 |

Arm | Intervention/treatment |
---|---|
Active Comparator: 1
1.5 mg bevacizumab single injection and on demand if leakage is persistent or recurs
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Device: subthreshold micropulselaser
on demand if leakage is persistent or recurs after initial treatment Drug: bevacizumab 1.5 mg initial intravitreal injection |
Active Comparator: 2
initial selective subthreshold micropulselasercoagulation and on demand if leakage is persistent or recurs
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Device: subthreshold micropulselaser
on demand if leakage is persistent or recurs after initial treatment |
No Intervention: 3
control
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- BCVA in EDTRS values [ Time Frame: 24 months ]
- OCT, leakage in FA, defects in satic perimetry [ Time Frame: 24 months ]

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Ages Eligible for Study: | 21 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion criteria:
- CSC of >4 months duration
Exclusion Criteria:
- History of macular or chorioretinal inflammation
- Lens / corneal opacities

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00802906
Germany | |
ZAU Department of VR surgery | |
Frankfurt / Main, Hessen, Germany, 60590 |
Principal Investigator: | Michael Koss, MD | ZAU Department of Vitreoretinal surgery |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Michael Koss, PI, Johann Wolfgang Goethe University Hospital |
ClinicalTrials.gov Identifier: | NCT00802906 History of Changes |
Other Study ID Numbers: |
MK-RCS-2008 |
First Posted: | December 5, 2008 Key Record Dates |
Last Update Posted: | September 27, 2012 |
Last Verified: | September 2012 |
Keywords provided by Michael Koss, Johann Wolfgang Goethe University Hospital:
micropulselaserphotocoagulation bevacizumab CSC |
Additional relevant MeSH terms:
Central Serous Chorioretinopathy Retinal Diseases Eye Diseases Bevacizumab Angiogenesis Inhibitors |
Angiogenesis Modulating Agents Growth Substances Physiological Effects of Drugs Growth Inhibitors Antineoplastic Agents |