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NCT07638592Completed

Tirzepatide-Based Prehabilitation Before Elective Ventral and Incisional Hernia Repair in Patients With Obesity

Tirzepatide-Based Prehabilitation Before Elective Ventral and Incisional Hernia Repair in Patients With Obesity:A Prospective Multicenter Cohort Study With a Comparative Control Cohort

Source: ClinicalTrials.gov · Last updated 11 Jun 2026

Brief summary (registry, in English)

This study evaluated whether a 16-week weight-loss program using tirzepatide before elective ventral and incisional hernia surgery could improve surgical readiness and outcomes in patients with obesity. In this retrospective multicenter study, 109 patients entered the program, and 91 completed treatment and underwent surgery. Participants achieved an average weight loss of 13.8%, and all patients who completed the program reached the target weight required for surgery. Compared with a control group of obese patients who underwent hernia repair without pharmacological prehabilitation, the tirzepatide group experienced fewer postoperative wound-related complications.

Status (registry)
Completed
Study type
Observational
Enrollment
91 (actual)
First submitted
5 Jun 2026
Start date
1 Jan 2025
Primary completion date
1 Jun 2026
Lead sponsor
Azienda Sanitaria Locale Napoli 2 Nord
Diseases
Obesity
NCT number
NCT07638592

What you commit to

  • Study type: Observational
  • Participants enrolled: 91
  • From 1 Jan 2025 to the primary completion date, 1 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindication to tirzepatide (personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2; prior pancreatitis; severe gastrointestinal disease; pregnancy or lactation) Ongoing treatment with another anti-obesity medication
  • Prior bariatric surgery within the preceding 12 months

Other

  • Emergency presentation or incarcerated/strangulated hernia
  • Hernia requiring posterior component separation or transversus abdominis release (TAR)
  • Inability to comply with follow-up

Who the study is looking for

  • Age ≥ 18 years
  • Body mass index (BMI) ≥ 30 kg/m²
  • Elective primary ventral or incisional midline hernia
  • European Hernia Society (EHS) width W2 (4-10 cm) or W3 (\> 10 cm)
  • Hernia amenable to a standard Rives-Stoppa retromuscular repair
  • Able and willing to comply with the prehabilitation program and scheduled follow-up

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Francesco Pizza
Coordinator of this site? Confirm its status
NaplesItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.