Choroidal Thickness Measurements During Central Serous Chorioretinopathy (CSCR) Treatment

Choroidal Thickness Clinical Trial

Official title:
Choroidal Thickness Measurements During CSCR Treatment Applying EDI-OCT Technology

Status Completed

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01610804
Study type	Observational
Source	University Hospital Regensburg
Contact
Status	Completed
Phase	N/A
Start date	April 2011
Completion date	May 2012

View Details

See also
	Status	Clinical Trial	Phase
	Not yet recruiting	`NCT03160690` - Changes in Choroidal Thickness After Non Penetrating Deep Sclerectomy	N/A
	Completed	`NCT03050073` - Choroidal Thickness Association With Primary Angle Closure