Skip to content

Efficacy Study of Δ9-THC to Treat Chronic Abdominal Pain

CompletedPhase 2NCT01318369
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

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.

Study details

Official title
The Safety, Tolerability, and Analgesic Efficacy of Δ9-THC (Namisol®) in Chronic Pancreatitis Patients Suffering From Persistent Abdominal Pain
Conditions
Interventions
  • Drug: Namisol
  • Drug: Diazepam
Sponsor
Radboud University Medical Center
Start date
2011-10
Primary completion
2013-05
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Netherlands
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
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.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01318369