Status:

RECRUITING

Effect of Abdominal Wall Injections on Abdominal Pain

Lead Sponsor:

Oregon Health and Science University

Conditions:

Anterior Cutaneous Nerve Entrapment Syndrome

Eligibility:

All Genders

18-100 years

Phase:

PHASE4

Brief Summary

This is a prospective cohort study of outpatient adults with chronic abdominal wall pain receiving abdominal wall injections, as part of their usual care, with lidocaine. Subjects will be recruited at...

Detailed Description

This is a prospective cohort study of outpatient adults with chronic abdominal wall pain who receive abdominal wall injections with lidocaine at an academic medical center. Thirty patients will be enr...

Eligibility Criteria

Inclusion

  • Localized abdominal wall pain
  • Average daily pain (7-day recall) ≥ 3 on a scale of 0-10
  • Suspected abdominal wall etiology for abdominal pain
  • Positive Carnett's sign or pain near an incisional site
  • 18 years of age or older

Exclusion

  • Suspected visceral etiology for the abdominal pain
  • Severe allergy to lidocaine
  • Unwillingness or inability to provide informed consent
  • Low probability of follow-up
  • Abdominal wall hernia noted at the point of pain
  • History of trigger point injections for abdominal pain
  • Bleeding disorder
  • Pregnancy, incarceration or decisionally impaired

Key Trial Info

Start Date :

January 1 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2025

Estimated Enrollment :

45 Patients enrolled

Trial Details

Trial ID

NCT06121466

Start Date

January 1 2023

End Date

December 1 2025

Last Update

September 2 2025

Active Locations (2)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (2 locations)

1

OHSU

Portland, Oregon, United States, 97239

2

Oregon Health Sciences University

Portland, Oregon, United States, 97239