Clin2
NCT04779918Possibly a fitRecruiting

Robotic hernia repair using OviTex implant mesh

Hernia, VentralHernia, Inguinal

Part of Digestive system clinical trials.

This trial studies whether using a specific implant “mesh” (OviTex) during robotic hernia surgery helps patients heal well and report less pain and better quality of life over time. It may be an option if you have a ventral or inguinal hernia planned for elective robotic repair.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
160 people
Ages
21 years and older
Study type
Interventional

Who can take part

  • You have a ventral or inguinal hernia that needs surgery with an implant to reinforce or replace weakened tissue
  • Your surgery is planned as an elective robotic hernia repair using one of the listed OviTex implant options
  • The needed implant size is within the study’s limits (larger allowed for one specific implant type)
  • Your wound is expected to be clean, clean-contaminated, or contaminated (not dirty-infected)
  • You are age 21 or older and can sign consent and complete pain and quality-of-life questionnaires
  • You can return for follow-up visits for the full study period (about two years)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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