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Bevacizumab Versus Micropulse in Central Serous Chorioretinopathy (CSC)

J

Johann Wolfgang Goethe University Hospital

Status

Completed

Conditions

Central Serous Chorioretinopathy

Treatments

Device: subthreshold micropulselaser
Drug: bevacizumab

Study type

Interventional

Funder types

Other

Identifiers

NCT00802906
MK-RCS-2008

Details and patient eligibility

About

The purpose of this study is to evaluate the clinical efficacy of an initial subthreshold retinal micropulselasercoagulation versus a single intravitreal 1.5mg bevacizumab injection in central serous choriretinopathy, as the micropulse will selectively treat the damaged RPE to induce reproliferation of healthy RPE cells, whereas the intravitreal injection should non-selectively stop the RPE leakage.

Full description

To evaluate the clinical efficacy of an initial subthreshold retinal micropulselasercoagulation in twelve eyey per group versus a single intravitreal 1.5mg bevacizumab injection in central serous choriretinopathy, as the micropulse will selectively treat the damaged RPE to induce reproliferation of healthy RPE cells. BCVA in EDTRS score, OCT, and leakage in FLA, static perimetry of both groups will be correlated to a control group without treatment over 10 months.

Enrollment

12 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • CSC of >4 months duration

Exclusion criteria

  • History of macular or chorioretinal inflammation
  • Lens / corneal opacities

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

12 participants in 3 patient groups

1
Active Comparator group
Description:
1.5 mg bevacizumab single injection and on demand if leakage is persistent or recurs
Treatment:
Device: subthreshold micropulselaser
Drug: bevacizumab
2
Active Comparator group
Description:
initial selective subthreshold micropulselasercoagulation and on demand if leakage is persistent or recurs
Treatment:
Device: subthreshold micropulselaser
3
No Intervention group
Description:
control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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