Preventing incisional hernias after kidney transplantation
Prevention of Incisional Hernia After Renal Transplantation Using ProGrip Mesh
This study is testing if using a special mesh during kidney transplant surgery can help prevent hernias from forming afterward in patients receiving their first transplant.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 160 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal Academic / other |
| Locations | 1 site (Madrid) |
| Trial ID | NCT04794582 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of using ProGrip™ Self-Gripping Polyester Mesh for reinforcing laparotomy closure in patients undergoing their first kidney transplant. The study will randomly assign participants to assess the reduction in the incidence of incisional hernias two years post-transplantation. Given the increased risk of hernias in transplant recipients due to immunosuppressive therapy, this approach seeks to improve surgical outcomes and reduce postoperative complications. The trial will monitor participants for hernia development through physical examinations and imaging tests.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals who are scheduled to receive their first kidney transplant.
Not a fit: Patients who are receiving a second or successive renal transplant will not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce the incidence of incisional hernias in kidney transplant patients, leading to improved recovery and quality of life.
How similar studies have performed: While there is limited scientific evidence on this specific approach, previous studies have indicated a potential benefit of mesh reinforcement in reducing hernia rates, making this a promising area of investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Candidate for first kidney transplant Exclusion Criteria: * Patient receiving a second or successive renal transplant.
Where this trial is running
Madrid
- Hospital Universitario Ramón y Cajal — Madrid, Spain (Recruiting)
Study contacts
- Principal investigator: Victoria Gomez — Fundación para la Investigación Biomédica del Hospital Unive
- Study coordinator: Gomez
- Email: vgomezd69@gmail.com
- Phone: +34670795972
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.