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The use of microscopic optical coherence tomography in patients with Fuchs corneal endothelial dystrophy

Conditions
H18.5
Hereditary corneal dystrophies
Registration Number
DRKS00018848
Lead Sponsor
niversitätsklinikum Köln
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting withdrawn before recruiting started
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients
- male, female, older than 18 years, able to give written consent
- availaben written consent
- diagnosed with Fuches endothelial dystrophy
- culture time maximum 50 days, preferably less than 35 days
- consent of the donor or next relative for usage in this study
- not eligible for transplantation

Exclusion Criteria

Patient:
- known infectious diseases
- other ophthalmological diseases than FED or Cataracta
- no consenct for scientific studies
- culture lenght > 50 days

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To obtain detailed information about ultrastructural changes in cornea explants of healthy individuals and FED-patients.<br>The corneas of FED-patients are obtained when these patients undergo surgical treatment (Descemet membrane endothelial keratoplasty). The corneas of healthy individuals are obtained from the Gewebebank Mecklenburg-Vorpommern. These are corneas stored for scientific purpose.
Secondary Outcome Measures
NameTimeMethod
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