Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07422584

Cytokine Response to Abdominal Wall Reconstruction

Led by Northwestern University · Updated on 2026-02-20

25

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Cytokine Response to Abdominal Wall Reconstruction

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Scheduled to undergo open retromuscular ventral hernia repair
  • Able to provide written informed consent
  • Adults aged 18 years or older (healthy controls)
  • No known inflammatory, autoimmune, or immunologic disease (healthy controls)
  • Able to provide written informed consent (healthy controls)
Not Eligible

You will not qualify if you...

  • Emergent or urgent cases
  • Pregnancy
  • Chronic systemic steroid use or immunosuppressive therapy
  • Active infection at the time of enrollment
  • Known autoimmune or inflammatory disease
  • End-stage organ failure
  • Abdominal surgery within the preceding 60 days

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Northwestern Memorial Hospital

Chicago, Illinois, United States, 60611

Actively Recruiting

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Research Team

M

Megan Melland-Smith, MD

CONTACT

N

Nancy Ly, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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