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Management and Outcome of Mesh Infection After Abdominoplasty in a Tertiary Care Centre

Management and Outcome of Mesh Infections After Abdominoplasty in a Tertiary Care Center in France

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06682091
Acronym
MOCOMI
Enrollment
209
Registered
2024-11-12
Start date
2013-01-01
Completion date
2023-01-01
Last updated
2024-11-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Infection

Keywords

mesh infection, abdominoplasty

Brief summary

Hernia repair is among most frequent surgical interventions. The use of abdominal mesh in hernia repair has become the Gold Standard strategy, reducing the risk of relapse. The mesh infection risk is estimated lower than 1% in simple situations, but can increase up to 20% in complicated patients. Risk factors are well known, but we lack data regarding the therapeutic strategies and outcomes. This study aims to describe the characteristics and management of abdominal mesh infections, and the related outcomes.

Interventions

None listed

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* parietal mesh infection * age \> 18

Exclusion criteria

* Non French speaking patients. * Persons under tutorship or curatorship.

Design outcomes

Primary

MeasureTime frameDescription
Treatment failure.Retrospective analysis from initial treatment to any treatment failure within 2010 to 2023Clinical failure = persistance of the infection. Time of failure is the time of change of therapeutic strategy.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026