Study of the Anatomical and Functional Recovery and Quality of Life of Patients Undergoing Corneal Transplantation
- Conditions
- Cornea Transplant
- Registration Number
- NCT06830538
- Brief Summary
Evaluate the well-being of patients and clinicl outcomes of the cornea after transplantation
- Detailed Description
The study aims to evaluate patients affected by corneal diseases who will undergo corneal transplantation.
The evaluation will be carried out pre and post transplantation to evaluate the clinical outcome of the patients and the quality of life and functional anatomical recovery.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 2000
- be eighteen years old
- diagnosis of corneal disease with prescription of surgical treatment of corneal transplantation
- sign the informed consent
- no exclusion criteria
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual-functional recovery after corneal transplant postoperatively at 7 days, 30 days, 3 months, and 12 months. Visus examination
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.
- Secondary Outcome Measures
Name Time Method Patients's quality of life One week before surgery and at seven days, thirty days, three months, six months, one year, two years, three years, and four years after surgery. Administration to patients of Schedule for the Evaluation of Individual Quality of Life (SEI-QoL) questionnaire
Related Research Topics
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Trial Locations
- Locations (1)
IRCCS Azienda Ospedaliero-Universitaria di Bologna
🇮🇹Bologna, Italy