Evaluating recovery and quality of life after corneal transplantation
Prospective Observational Spontaneous Study of Anatomical, Functional and QoL Recovery of Patients Undergoing Corneal Transplantation
This study looks at how well people feel and recover after having corneal transplant surgery for eye problems.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 1 site (Bologna) |
| Trial ID | NCT06830538 on ClinicalTrials.gov |
What this trial studies
This study evaluates the well-being and clinical outcomes of patients undergoing corneal transplantation due to corneal diseases. It involves assessing patients before and after the surgery to determine the functional anatomical recovery and overall quality of life. The observational nature of the study allows for a comprehensive understanding of the impact of the procedure on patients' lives.
Who should consider this trial
Good fit: Ideal candidates are adults aged eighteen and older diagnosed with corneal disease requiring surgical treatment.
Not a fit: Patients who do not have a diagnosis of corneal disease or do not require corneal transplantation may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into improving patient care and outcomes following corneal transplantation.
How similar studies have performed: While similar studies have been conducted, this specific observational approach focusing on quality of life post-transplantation may provide novel insights.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Bologna
- IRCCS Azienda Ospedaliero-Universitaria di Bologna — Bologna, Italy (Recruiting)
Study contacts
- Principal investigator: Luigi Fontana, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Luigi Fontana, MD
- Email: luigi.fontana6@unibo.it
- Phone: +390512142832
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.