Efficacy Study of Δ9-THC to Treat Chronic Abdominal Pain

• Status: Completed
• Trial end date: 2013-05-01
• Target enrollment: 0
• Participant gender: All

Summary

The main goal of this trial is to study the efficacy of Namisol® after a single dose of Δ9-THC in the treatment of pain resulting from chronic pancreatitis. Objective measures of pain processing, e.g. encephalography (EEG) and quantitative sensory testing (QST), are included to provide insight in underlying nociceptive processing.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Radboud University
• Treatments: Diazepam; Dronabinol

Criteria

Inclusion Criteria:

• Patient has chronic pancreatitis, diagnosed using the Marseille and Cambridge Classification System (addendum II).37

• Patient suffers from chronic abdominal pain typical for pancreatitis, meet the criteria for chronic pain according ISAP (intermittent or persistent pain on a daily basis in at least 3 months)38, and consider their pain must as severe enough for medical treatment (average NRS ≥ 3).

• Patient in the opioid group takes stable doses of opioids, e.g. morphine or tramadol, for the past 2 months on the day of screening. Stable dose intake is defined as a daily equivalent sum of opioid intake according medical prescription within a small deviation range as judged by the (principal) investigator.

• Patient in the non-opioid group does not take any opioids for the past 2 months on the day of screening.

Exclusion Criteria:

• Patient used any cannabinoid (by smoking cannabis or oral intake) for at least one year on the day of screening.

• Patient does not feel a pinprick test in the lower extremities, due to affected sensory input (e.g. neuropathy as a result of diabetes mellitus).

• Patient has a body mass index (BMI) below 18 or above 31.2 kg/m2.

• Patient suffers from serious painful conditions other than chronic pancreatitis or had any major pre-existing chronic pain syndrome.

• Patient has a (history of) a significant medical disorder that, in the opinion of the investigator, may interfere with the study or may pose a risk for the patient.

• Patient uses any kind of concomitant medication that, in the opinion of the investigator, may interfere with the study or may pose a risk for the patient (e.g. HIV antivirals).

• Patient takes amitriptyline on a daily basis.

• Patient takes more than 20 mg benzodiazepines 6 hours prior or following intake of study medication (11 hour am) according prescription.