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NCT Number: NCT07192978

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

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.

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Key information

Conditions

Incisional Hernia Hernia Pathologic Processes Pathological Conditions, Anatomical Pathological Conditions, Signs and Symptoms Postoperative Complications

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

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

Strasbourg, 67091, France

Location status: Recruiting

Location contact

Aurélien VILLEMIN, MD

SUB_INVESTIGATOR

Benoit Romain

CONTACT

[email protected]

33 3.88.12.89.37

Benoit Romain, MD, PhD

PRINCIPAL_INVESTIGATOR

Florian SECKLER, MD

SUB_INVESTIGATOR

Sidney LAZERT, MD

SUB_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

Complications according to the Comprehensive Complication Index (CCI)

Time frame: Day 1 postoperatively

The Comprehensive Complication Index (CCI) Score takes into account all postoperative complications and allows them to be expressed by a score ranging from 0 (no complications) to 100 (death).

Study contacts

Contact information is provided by the study sponsor or research team.

Benoit Romain, MD, PhD

CONTACT

[email protected]

33 3.88.12.89.37

Sponsors and collaborators

Lead sponsor

University Hospital, Strasbourg, France

Other

Registry information

Acronym: EVENTEST

Important dates

Study start: 2025
Primary completion: 2026
Study completion: 2026
First posted: Sep 25, 2025
Registry last updated: Sep 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Recruiting