Effect of Abdominal Wall Injections on Abdominal Pain
Recruiting
Phase 4Interventional Study
Anterior Cutaneous Nerve Entrapment Syndrome
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 100
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
45 (estimated)
Sponsor
Oregon Health and Science University · Other
Who this trial is looking for
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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 Criteria:
* Suspected visceral etiol…
Inclusion Criteria:
* 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 Criteria:
* 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
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