Does Preoperative Physical Activity Predict Postoperative Complications After Incisional Hernia Repair ?
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Incisional Hernia. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
Patients with abdominal wall incisional hernia often have numerous comorbidities, making management complex. To date, no study has described the relationship between preoperative physical activity and the occurrence of complications, particularly severe ones, after incisional hernia repair. The research hypothesis is that "patient fragility" related to physical inactivity and comorbidities is a poor prognostic factor for the occurrence of complications after incisional hernia repair and a source of more severe complications.
Primary outcome measures
- Complications according to the Comprehensive Complication Index (CCI) [Time frame: Day 1 postoperatively]
Eligibility criteria
Inclusion criteria
- Adult (≥18 years old)
- Subject operated on at the HUS between January 6, 2021 and October 24, 2024
- Midline eventration
- Placement of a prosthetic reinforcement
Exclusion criteria
\- Subject (and/or their legal representative, if applicable) who has expressed their opposition to the reuse of their data for scientific research purposes
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
France · 1 center
- Service de cchirurgie générale & digestive - CHU de Strasbourg - France — Strasbourg
Identifiers
NCT: NCT07192978 · 9768