H16.0 H16.8 H16.9
Conditions
Interventions
Group 1: The present study is designed as a retrospective observational study. No study-related intervention is performed.
Clinical routine data of patients who underwent partial or complete conjunct
Sponsors
St. Johannes Hospital Dortmund, Klinik für Augenheilkunde
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who underwent partial or complete conjunctival flap surgery between 2013 and 2023 at the Department of Ophthalmology, St. Johannes Hospital Dortmund.
Exclusion criteria
Exclusion criteria: No specific exclusion criteria are defined, as all patients who underwent conjunctival flap surgery within the defined study period are included, provided sufficient clinical documentation is available.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome is the treatment success defined as the absence of severe postoperative surgical interventions (e.g., keratoplasty or enucleation) following conjunctival flap surgery. This parameter is assessed during the entire follow-up period. Data are collected retrospectively from clinical routine documentation (medical records and surgical reports). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes include postoperative complications (e.g., conjunctival flap retraction), the need for additional surgical interventions, and functional outcomes (e.g., visual acuity and intraocular pressure). In addition, preoperative risk factors, comorbidities, and previous surgeries, as well as their potential impact on treatment success, are analyzed. Data are collected retrospectively from clinical routine documentation. | — |
Countries
Germany
Contacts
Public ContactHarald Schilling
Klinik für Augenheilkunde, St. Johannes-Hospital Dortmund
Outcome results
None listed