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Trial Comparing Tack Versus Histoacryl Mesh Fixation After Endoscopic TEP(Total Extraperitoneal) Repair for Bilateral Inguinal Hernia

Taiwan100 participantsStarted 2016-11

Plain-language summary

This prospective randomized trial is performed to analyze the post-operative pain (acute and chronic) after endoscopic TEP repair after bilateral inguinal hernia repair.

Who can participate

Age range18 Years – 85 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients present with clinical bilateral inguinal hernias And feasible for general anesthesia Exclusion Criteria: * Patient preference for either fixation technique, refusal to participate, previous major lower abdominal surgery, concomitant surgical procedures other than hernia repair, and history of allergy to Histoacryl.

What they're measuring

acute post-operative pain with VAS

Timeframe: 6 hours after OP

Trial details

NCT IDNCT02932033

SponsorTaipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-10

View on ClinicalTrials.gov More Inguinal Hernia trials