Choroidal Thickness Measurements During Central Serous Chorioretinopathy (CSCR) Treatment

University Hospital Regensburg

Status: Completed

Conditions: Choroidal Thickness

Study type: Observational

Funder types: Other

Identifiers

NCT01610804

CSCR2011

Details and patient eligibility

About

The purpose of this study is to determine changes in choroidal thickness in patients with Central Serous Chorioretinopathy (CSCR) during the first 3 months after initial diagnosis via Enhanced-Depth-Imaging-Spectral-Domain-Optical-Coherence-Tomography (EDI-OCT).

Study hypothesis: Since exudative changes in the choroid seem to constitute the primary pathology of CSCR, changes in choroidal thickness compared to healthy eyes should be present and be visible using EDI-OCT.

Enrollment: 18 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients with initial diagnosis of CSCR and no treatment so far

Exclusion criteria

• Therapy (drugs/laser) due to CSCR

Trial design

18 participants in 2 patient groups

CSCR-Patients

Description:

Patients suffering from Central Serous Chorioretinopathy

Healthy Subjects

Description:

Healthy subjects with (assumed) normal choroidal thickness