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Synthetic Mesh Explant Study

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The Washington University

Status

Completed

Conditions

Materials Testing
Histology
Herniorrhaphy
Polypropylene
Humans
Polytetrafluoroethylene

Study type

Observational

Funder types

Other

Identifiers

NCT01880021
2010-12735

Details and patient eligibility

About

The purpose of this study is to determine whether synthetic hernia mesh materials undergo physical and/or chemical changes while in the body.

Enrollment

111 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 yrs
  • Previous placement of hernia mesh material
  • Current need for excision of previous mesh placement or Current need for intra-abdominal surgical procedure

Exclusion criteria

  • Age < 18 yrs
  • No retained mesh prosthetic.
  • Non surgical candidate
  • Prisoner

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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