Actively Recruiting
Effect of Abdominal Wall Injections on Abdominal Pain
Led by Oregon Health and Science University · Updated on 2025-09-02
45
Participants Needed
2
Research Sites
152 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Effect of Abdominal Wall Injections on Abdominal Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Localized abdominal wall pain
- Average daily pain (7-day recall) 2 3 on a scale of 0-10
- Suspected abdominal wall cause for abdominal pain
- Positive Carnett's sign or pain near an incisional site
- 18 years of age or older
You will not qualify if you...
- Suspected visceral cause for the abdominal pain
- Severe allergy to lidocaine
- Unwillingness or inability to provide informed consent
- Low probability of follow-up
- Abdominal wall hernia at the point of pain
- History of trigger point injections for abdominal pain
- Bleeding disorder
- Pregnancy, incarceration or decisionally impaired
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
OHSU
Portland, Oregon, United States, 97239
Actively Recruiting
2
Oregon Health Sciences University
Portland, Oregon, United States, 97239
Actively Recruiting
Research Team
S
Sophia Lichenstein-Hill, DNP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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