Effect of Abdominal Wall Injections on Abdominal Pain

Part of paid clinical trials in Portland, Oregon.

Sponsor
Oregon Health and Science University
Study ID
NCT06121466
Phase
PHASE4
Status
Recruiting

Conditions

  • Anterior Cutaneous Nerve Entrapment Syndrome

Eligibility Criteria

Sex
ALL
Age
18 Years - 100 Years
Healthy Volunteers
Accepted

Interventions

  • Abdominal wall injections with lidocaine 2% — DRUG
    Injections will be administered for patient who are identified as having abdominal wall pain.

Study Details

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 the outpatient gastroenterology clinic at OHSU.

Key Dates

Start date
Jan 1, 2023
Status verified
Aug 2025
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025

Study Design

Enrollment
45 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Abdominal wall injections for abdominal wall pain
    Patients with abdominal pain who are suspected of having abdominal wall pain.

Primary Outcome Measure

1) To measure the change in abdominal wall pain 1-week, 1-month and 3-months following abdominal wall injections, with improvement defined as a 50% reduction in baseline pain score measured using an 11-point numeric scale. [ Time Frame: 12 weeks ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
OHSUPortlandOregon97239
Sophia Lichenstein-Hill
5034944373
Oregon Health Sciences UniversityPortlandOregon97239
Oregon HS University
5034944373

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