Investigating infections related to abdominal wall prostheses
Early Abdominal Wall Prosthesis Infections: Epidemiology, Risk Factors and Factors Linked to Recovery
This study looks at infections that can happen after surgery with abdominal wall mesh to see what causes them and how to better manage these issues for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Strasbourg, France Academic / other |
| Locations | 1 site (Strasbourg) |
| Trial ID | NCT06498245 on ClinicalTrials.gov |
What this trial studies
This observational study aims to analyze the epidemiology and risk factors associated with infections of abdominal wall prostheses. By reviewing data from approximately 500 patients who underwent incisional hernia repair with prosthesis installation at the University Hospital of Strasbourg, the study seeks to identify the characteristics of these infections, including the types of microorganisms involved and the timing of infection onset. The goal is to optimize management strategies for these infections, which are known to complicate recovery and increase morbidity.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have undergone surgery for incisional hernia repair with abdominal wall prosthesis installation at the University Hospital of Strasbourg between January 2017 and July 2023.
Not a fit: Patients who have expressed opposition to the reuse of their medical data for research purposes will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management and treatment strategies for patients suffering from abdominal wall prosthesis infections.
How similar studies have performed: While there is limited literature on this specific topic, similar studies investigating surgical infections have shown varying degrees of success in improving treatment protocols.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Major subject (≥18 years old) * Subject operated on at the HUS in the department of Pr. Rohr between January 1, 2017 and July 26, 2023 * Operation of an incisional hernia cure with installation of an abdominal wall prosthesis * Absence of written opposition in the subject's medical file to the reuse of their data for scientific research purposes. Exclusion Criteria: * Subject having expressed his opposition to the reuse of his data for scientific research purposes.
Where this trial is running
Strasbourg
- Service des Maladies Infectieuses et Tropicales - CHU de Strasbourg - France — Strasbourg, France (Recruiting)
Study contacts
- Study coordinator: Victor GERBER, MD
- Email: victor.gerber@chru-strasbourg.fr
- Phone: 33.3.88.11.67.68
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.