Pregabalin for Abdominal Pain From Adhesions

Stopped early · Phase 4 · Has a placebo group

Conditions studied: Abdominal Pain, Surgical Adhesions

In brief

The purpose of this study is to evaluate if pregabalin demonstrates significant reduction in abdominal pain from adhesions.

Key facts

Study ID

NCT00310765

Run by

Henry Ford Health System

People needed

18

Starts

2006-03-01

Expected to finish

2008-08-01

Last updated by the study team

2023-10-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Must have history of prior surgery and documented adhesions during laparoscopy or open laparotomy within 5 years
• Must have undergone an evaluation to exclude other causes of abdominal pain
• Abdominal pain must be present for greater than three months duration

You may not qualify if…

• Patients that are pregnant or breast feeding
• Prior treatment with gabapentin, pregabalin or demonstrated sensitivity to these drugs
• Patients who are immunocompromised
• Patients with significant hepatic or renal insufficiency, or any significant hematologic disorder
• History of illicit alcohol or drug abuse within one year
• Documented serious or unstable medical or psychological condition
• Malignancy within the past 5 years other than in situ squamous cell carcinoma of the skin

Where it is running

• Henry Ford Health System — West Bloomfield, Michigan, United States

Full record on ClinicalTrials.gov

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