Clinical Trials in Italy / NCT06830538
Recruiting
Observational
Study of the Anatomical and Functional Recovery and Quality of Life of Patients Undergoing Corneal Transplantation
NCT06830538 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Cornea Transplant
Study summary
Evaluate the well-being of patients and clinicl outcomes of the cornea after transplantation
Eligibility
Inclusion Criteria:
* be eighteen years old
* diagnosis of corneal disease with prescription of surgical treatment of corneal transplantation
* sign the informed consent
Exclusion Criteria:
* no exclusion criteria
Primary outcome measure(s)
- Anatomical recovery after corneal transplant — postoperatively at 7 days, 30 days, 3 months, and 12 months.
Anatomical recovery will be assessed by the regularity of the cornea. - Visual-functional recovery after corneal transplant — postoperatively at 7 days, 30 days, 3 months, and 12 months.
Visus examination
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | Bologna | Italy | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06830538 on ClinicalTrials.gov ↗ ← All trials in Italy