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NCT07422584

Cytokine Response to Abdominal Wall Reconstruction

Recruiting now Last updated 20 February 2026
What this trial tests

trial testing Not applicable- observational study in Incisional Ventral Hernia in 25 participants. Currently enrolling.

Timeline
3 February 2026
Primary endpoint
5 February 2027
5 March 2027

Quick facts

Lead sponsorNorthwestern University
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment25
Start date3 February 2026
Primary completion5 February 2027
Estimated completion5 March 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Northwestern University

Who can join

18 and older, any sex, with Incisional Ventral Hernia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective, observational translational study of patients undergoing major abdominal wall reconstruction with primary fascial closure. The project integrates perioperative cytokine profiling, direct measurement of intra-abdominal pressure, and detailed clinical outcomes to define the biologic and physiologic consequences of high-tension closure. The study includes three cohorts: 1) Healthy controls (N=5), 2) High-tension fascial closure AWR patients (N=10), 3) Low-tension fascial closure AWR patients (N=10). Fascial closure tension will not be altered for the purpose of the study and will be determined by the operating surgeon as part of routine clinical decision-making.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Not applicable- observational study

Trials testing the same drug.

Other Northwestern University trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing