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ACute Treatment of Incisional Ventral Hernia

NCT05620121 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2024-01-30

No results posted yet for this study

Summary

This observational, retrospective study aims to examine surgical outcomes in non-elective surgery for incisional hernia.

The main questions it aims to answer are:

* 30-day morbidity
* short- and long-term surgical outcomes

Data will be retrospectively collected from participating centers and compared. Researchers will compare surgical outcomes of the minimally invasive and laparotomic approaches to see if there are relevant differences in surgical outcomes.

Conditions

  • Incisional Hernia

Interventions

PROCEDURE

Surgery for Incisional hernias

Laparoscopic and laparoscopic abdominal wall repair for Incisional Hernia with/without prosthetic material in urgent/emergent settings, with/without direct closure of the defect (IPOM and IPOM +).

Sponsors & Collaborators

  • Ospedale San Camillo

    lead OTHER

Principal Investigators

  • Lorenzo Crepaz · Ospedale San Camillo

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-15
Primary Completion
2024-04-30
Completion
2024-04-30

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05620121 on ClinicalTrials.gov