Actively Recruiting

Age: 18Years +
All Genders
ID07192978

Does Preoperative Physical Activity Predict Postoperative Complications After Incisional Hernia Repair?

Led by University Hospital, Strasbourg, France · Updated on 2025-09-25

100

Participants Needed

1

Research Sites

1 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients with abdominal wall incisional hernia often face complex management challenges due to multiple health conditions. This observational study investigates whether preoperative physical activity levels and patient fragility, influenced by inactivity and other health issues, relate to the risk and severity of complications following incisional hernia repair. The study observes adults who have undergone midline incisional hernia surgery with prosthetic reinforcement at a hospital. It aims to track postoperative complications using the Comprehensive Complication Index (CCI) measured on the first day after surgery. No interventions or treatments are assigned, as this is an observational research. Participants' medical records and surgical outcomes will be reviewed to assess complication rates and severity. Researchers will analyze how pre-surgery physical activity and fragility relate to postoperative recovery. The study runs from September 2025 to September 2026, with participants having surgery recorded between January 2021 and October 2024.

CONDITIONS

Brief Title

Does Preoperative Physical Activity Predict Postoperative Complications After Incisional Hernia Repair ?

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Had midline incisional hernia surgery with prosthetic reinforcement at the University Hospital, Strasbourg, between January 6, 2021 and October 24, 2024
Not Eligible

You will not qualify if you...

  • Individuals who oppose the reuse of their medical data for scientific research purposes, including their legal representatives if applicable
  • Lack of consent for data use in research purposes if applicable
  • Any other opposition to participation based on data privacy concerns as stated by the patient or legal representative if applicable
  • Participants without midline incisional hernia or prosthetic reinforcement surgery are excluded

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 1 day postoperatively

Participants who have undergone midline incisional hernia surgery with prosthetic reinforcement are observed to assess postoperative complications.

1 visit (in-person, Day 1 postoperatively)

Trial Site Locations

Total: 1 location

1

Service de cchirurgie générale & digestive - CHU de Strasbourg - France

Strasbourg, France, 67091

Actively Recruiting

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Research Team

B

Benoit Romain, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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