Clinical Trial

Cytokine Response to Abdominal Wall Reconstruction

Recruiting
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Summary
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.
Trial Details
NCT Number NCT07422584
Lead Sponsor Northwestern University
Conditions Incisional Ventral Hernia
Enrollment 25 participants
Start Date 2026-02-03
Primary Completion 2027-02-05 (estimated)
Study Completion 2027-03-05 (estimated)
Updated on ClinicalTrials.gov 2026-02-20