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Completed

NCT Number: NCT01318369

Efficacy Study of Δ9-THC to Treat Chronic Abdominal Pain

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Radboud University Nijmegen Medical Centre

Nijmegen, Gelderland, 6500 HB, Netherlands

About this study

The most important symptom in chronic pancreatitis (CP) is abdominal pain. Pancreatic pain is often recurrent, intense and long-lasting, and is extremely difficult to treat. Medical analgesic therapy is considered as first choice in pain management of CP, resulting in regularly prescription of opioids. The adverse consequences of prolonged opioid use, including addiction, tolerance and opioid induced hyperalgesia, call for an alternative medical treatment. Cannabis has been used to treat pain for many centuries. Delta-9-tetrahydrocannabinol (Δ9-THC), the psychoactive substance of the cannabis plant, has been shown in previous studies to be a promising analgesic. The development of Namisol®, a tablet containing purified Δ9-THC showing an improved and reliable pharmacokinetic profile, provides the opportunity to test the analgesic potential of Δ9-THC in favourable conditions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Namisol

Drug

Single dose delta-9-tetrahydrocannabinol

Other names: Dronabinol, THC

Diazepam

Drug

Diazepam single dose 5mg in subgroup non-opioid users and 10 mg in subgroup opioid users.

Primary outcomes

  1. Pain intensity (VAS pain)

    Time frame: Repeatedly; baseline until 6 hours after administration

    Pain intensity (VAS pain at rest and on movement)

Secondary outcomes

  1. EEG

    Time frame: Repeatedly; baseline until 6 hours after administration

    Spontaneous EEG and evoked potentials to noxious electrical stimuli

  2. QST

    Time frame: Repeatedly; baseline until 6 hours after administration

    Quantitative Sensory Testing, using pressure pain tolerance and electrical thresholds

  3. Body sway

    Time frame: Repeatedly; baseline until 6 hours after administration

    Static body sway

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Registry information

Official study title

The Safety, Tolerability, and Analgesic Efficacy of Δ9-THC (Namisol®) in Chronic Pancreatitis Patients Suffering From Persistent Abdominal Pain

Acronym: Delta-pain

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Mar 18, 2011
Registry last updated
Jul 9, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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