UnknownNot Applicable

Laparoscopic IPOM Plus vs. eTEP Trial

Russia72 participantsStarted 2023-02-14

Plain-language summary

The survey will compare primary and secondary outcomes of laparoscopic intraperitoneal onlay mesh (IPOM plus) and extended totally extraperitoneal (eTEP) repair for incisional hernia. The research hypothesis is the following: patients who underwent eTEP repair may experience 30% less pain, assessed on the NRS-11 scale by the end of postoperative day 1, compared with IPOM plus procedure

Who can participate

Age range18 Years

SexALL

See this in plain English?

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

Inclusion Criteria: * midline incisional hernia * defect width 2-6 cm * ASA I-II class * Elective hernia repair * Considered eligible for minimally invasive ventral hernia repair * Able to give informed consent * Able to tolerate general anesthesia Exclusion Criteria: * primary ventral herna * lateral hernia with/without midline * defect width more than 6 cm * refuse to give informed consent * prior mesh placement in the retrorectus space

What they're measuring

pain on postoperative day 1

Timeframe: postoperative day 1

Trial details

NCT IDNCT05528107

SponsorCity Clinical Hospital No.1 named after N.I. Pirogov

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12

Contact for this trial

Alexander Sazhin, professor

+79163904180 sazhin-av@yandex.ru

View on ClinicalTrials.gov More Incisional Hernia of Midline of Abdomen trials