Prospective observation study of patients with Chorioretinopathia centralis serous to identify hormonal and metabolic risk factors for chronificatio
Recruiting
- Conditions
- H35.7Separation of retinal layers
- Registration Number
- DRKS00013310
- Lead Sponsor
- Zentrum für AugenheilkundeUniklinik Köln
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Informed consent
Acute onset of clinical complaints in the last three weeks
Clinical diagnosis of CSC using retinal imaging
Exclusion Criteria
Lack of informed consent for the clinical trial
Presence of accompanying retinal diseases (e.g. high myopia >-8dpt, age-related macular degeneration, diabetic macular edema, macular dystrophy)
Unter 18 years old
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Identification of chronification (defined as persistence of the disease) of acutely occurring CRCS cases within 2 months
- Secondary Outcome Measures
Name Time Method ong-term observation of 1 years, identification of risk factors on the basis of questionnaires, retinal imaging, metabolic and hormonal risk factors