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Completed

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

Asset

Tirzepatide

Subcutaneous · GLP-1 / GIP dual

Listed sites

1

Recruiting sites

Enrollment

91

actual

Study population

Obesity / overweight

Key I/E criterion

BMI ≥30

Primary endpoint

Feasibility of tirzepatide-based prehabilitation

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT07638592
Org study ID2128112026

Timeline

Milestones

Study start2025-01-01actual
Primary completion2026-06-01actual
Study completion2026-06-01actual
Study first posted2026-06-10actual
Last update posted2026-06-11actual

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweight

Eligibility

Who can enroll

Minimum age18 Years
SexAll
Sampling methodNon probability sample

Study population text

Adults (≥ 18 years) with obesity (BMI ≥ 30 kg/m²) and an elective primary ventral or incisional midline hernia of European Hernia Society width W2-W3, amenable to a standard Rives-Stoppa retromuscular repair, managed at four high-volume abdominal wall surgery units. The prospective prehabilitation cohort comprises consecutive eligible patients who agreed to undergo a structured 16-week tirzepatide-based preoperative weight-optimization program before elective repair. The comparative control cohort comprises patients meeting the same age, BMI, hernia type, EHS width, and surgical-technique criteria who underwent elective repair without pharmacologic prehabilitation at the same centers over the preceding five years, identified from prospectively maintained institutional databases. Patients requiring emergency surgery, posterior component separation/transversus abdominis release, or with contraindications to tirzepatide were not included.

Inclusion criteria

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

Exclusion criteria

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

Endpoints (4)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Other (unclassified)
2
Weight & body composition
1
Other clinical outcomes
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Preoperative weight optimization

Time frame:16 weeks (from initiation of prehabilitation to surgery)

descriptive

Other clinical outcomes

1 endpoint
Primary/protocol endpoint

Feasibility of tirzepatide-based prehabilitation

Time frame:16 weeks (from initiation of prehabilitation to surgery)

descriptive

Other (unclassified)

2 endpoints
Secondary/protocol endpoint/low confidence

Composite surgical site occurrence

Time frame:90 days postoperatively

descriptive

Secondary/protocol endpoint/low confidence

Postoperative morbidity by Clavien-Dindo classification

Time frame:90 days postoperatively

descriptive

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.