Central Serous Chorioretinopathy: Etiology, Course and Prognosis

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Brief Title

Central Serous Chorioretinopathy: Etiology, Course and Prognosis

Official Title

Central Serous Chorioretinopathy: An Observational Study About Etiology, Course and Prognosis

Brief Summary

      Pathogenesis of central serous chorioretinopathy is not entirely understood yet, therefore
      further investigations are needed. During this study patients with an acute episode of
      central serous chorioretinopathy are observed with established ophthalmologic methods
      (multimodal imagine) every 6 weeks until subretinal fluid is reabsorbed to gain further
      insides in etiology, course and prognosis of this disease.
    

Detailed Description

      Patients with central serous chorioretinopathy are recruited from the Department of
      Ophthalmology at the Medical University of Vienna. All patients undergo ETDRS visual acuity
      measurement, Pelli-Robson contrast examination, Amsler-Grid testing, questionnaire testing,
      ophthalmologic examination, SD-OCT and polarization-sensitive OCT, fundus autofluorescence,
      fluorescein angiography, indocyanine-green angiography, fundus photo and microperimetry.
      Patients are re-examined after an interval of 6 weeks until subretinal fluid is entirely
      reabsorbed to gain further insides in etiology, course and prognosis of this disease.
    


Study Type

Observational


Primary Outcome

Clinical Outcome

Secondary Outcome

 Subclinical Data

Condition

Central Serous Chorioretinopathy



Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information



Estimated Enrollment

50

Start Date

April 2011

Completion Date

April 2013

Primary Completion Date

April 2013

Eligibility Criteria

        Inclusion Criteria:

          -  Signed informed consent form

          -  Age over 18 years

          -  acute episode of Central Serous Chorioretinopathy

          -  Symptoms for less than two weeks

          -  no treatment on study eye

        Exclusion Criteria:

          -  bad compliance

          -  protected patient group (pregnant women)
      

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Stefan Sacu, Ass.Prof.Dr., , 

Location Countries

Austria

Location Countries

Austria

Administrative Informations


NCT ID

NCT01378130

Organization ID

EK 180/2011


Responsible Party

Principal Investigator

Study Sponsor

Medical University of Vienna


Study Sponsor

Stefan Sacu, Ass.Prof.Dr., Principal Investigator, Department of Ophthalmology, Medical University of Vienna, Austria


Verification Date

April 2013