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Follow-up of Surgically Repaired Ventral (Abdominal) Hernias

Overview

About this study

The purpose of this study is to compare the results of different types of repair: open vs. laparoscopic, mesh vs. no mesh, and the type of mesh versus other mesh products over a 10 year period.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients who underwent ventral hernia repair, including incisional hernia repair, at Mayo Clinic and who consented to research.

Exclusion Criteria: 

  • None

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

David Farley, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

More about research at Mayo Clinic

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CLS-20308309

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