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Use of the Cannabinoid Nabilone for the Promotion of Sleep in Chronic, Non-Malignant Pain Patients

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified November 2005 by University Health Network, Toronto.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00384410
First Posted: October 6, 2006
Last Update Posted: October 6, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Valeant Pharmaceuticals International, Inc.
Information provided by:
University Health Network, Toronto
October 4, 2006
October 6, 2006
October 6, 2006
December 2005
Not Provided
The primary analysis variable will be the change in the mean of the sleep efficiency as measured by overnight polysomnography.
Same as current
No Changes Posted
• The key secondary efficacy variable will be the change in the total sleep time with nabilone treatment as compared to placebo
Same as current
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Use of the Cannabinoid Nabilone for the Promotion of Sleep in Chronic, Non-Malignant Pain Patients
Use of the Cannabinoid Nabilone for the Promotion of Sleep in Chronic, Non-Malignant Pain Patients: A Placebo-Controlled, Randomized, Crossover Insomnia Pilot Study
Sleep disturbance is perhaps one of the most prevalent complaints of patients with long-standing painful conditions. Nabilone is a medication that is approved by Health Canada as an anti-emetic (prevent vomiting) for patients undergoing chemotherapy. Nabilone, due to its sleep promoting properties, is sometimes prescribed by physicians to pain patients to help improve their sleep. However, there is no direct research evidence to either support or refute this practice. This study will investigate if nabilone is effective in improving sleep in insomnia and pain patients.

Rationale:

The current evidence suggests a sleep promoting effect of THC. Although, there is some support from pre-clinical and small sample size human studies suggesting a direct sleep enhancing effect, it remains unclear from the larger clinical trials, whether improved sleep is an epiphenomena secondary to improvements in the primary outcome measures ( i.e., pain, nausea or spasticity). There are no studies evaluating the sleep promoting effects of THC or analogues in patients with primary insomnia or objectively evaluating sleep at baseline and following treatment with THC or analogues in patients suffering from chronic pain disorder and insomnia. Cannabinoids have the potential of simultaneously improving sleep and lessening chronic, non-malignant pain, thereby interrupting the vicious cycle of pain and sleep disturbance. An investigation of the efficacy of cannabinoids in treating insomnia in chronic, non-malignant pain patients is therefore warranted.

Research Question:

To evaluate if nabilone (Cesamet) is effective in improving sleep in patients with insomnia and chronic, non-malignant pain

Interventional
Phase 2
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double
Primary Purpose: Treatment
  • Pain
  • Insomnia
Drug: Nabilone
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
16
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Inclusion Criteria

  • History of insomnia and chronic, non-malignant pain.
  • Patient not currently being prescribed opiates for pain management
  • Subject has no known clinically significant abnormal vital signs or other significant clinical findings at screening.

Exclusion criteria

  • Patients with a history of sensitivity of cannabinoids.
  • Patients currently taking hypnotics, psychotomimetic substances, CNS depressants or tricyclic antidepressants that may increase the CNS-depressant effects of nabilone.
  • Patients with active cardiac disease or respiratory disorders.
  • Patients with a history of psychotic reactions, schizophrenia, bipolar disorder or any serious untreated mental disorder.
  • Presence of untreated sleep disorder (other than insomnia) as detected using the screening overnight PSG.
  • Alcohol or substance abuse (according to DSM-IV) during the last 6 months prior to baseline.
  • Patients with liver disease that may interfere with the clearance of nabilone.
  • Patients who are nursing, pregnant or likely to become pregnant throughout the course of the study. During the study, female patients will be asked to use an effective method of birth control.
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
 
NCT00384410
NAB-20051
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University Health Network, Toronto
Valeant Pharmaceuticals International, Inc.
Principal Investigator: Colin M. Shapiro, MBBCh, PhD University Health Network, Toronto
University Health Network, Toronto
November 2005

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP