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| Sponsor: | University of Heidelberg |
|---|---|
| Collaborators: |
Central Institute of Mental Health, Mannheim University of Mannheim Academic City Hospital, Germany BG-clinics Ludwigshafen Germany |
| Information provided by: | University of Heidelberg |
| ClinicalTrials.gov Identifier: | NCT00176163 |
Purpose
It is known, that a so called "pain memory" usually evolves in chronic pain syndromes which both aggravates the disorder and modifies the patients pain perception. Thus, the principal object of pain therapy is to "delete" this dysfunctional pain memory. The combination of medication, physiotherapy and psychological therapy seems to be the most effective treatment. This study investigates the effect of a concomitant Dronabinol medication (Cannabinoid) on the effectiveness of behavioral therapy. It is hypothesized that the combination of behavioral therapy and Dronabinol will be most effective in deleting the pain memory.
| Condition | Intervention | Phase |
|---|---|---|
|
Fibromyalgia Back Pain |
Behavioral: Operant behavioral treatment; Drug: THC |
Phase II |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Factorial Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Supporting Effect of Dronabinol on Behavioral Therapy in Fibromyalgia and Chronic Back Pain |
| Estimated Enrollment: | 240 |
| Study Start Date: | August 2005 |
| Estimated Study Completion Date: | May 2009 |
This study investigates the combination of operant behavioral treatment and Cannabinoid medication in patients with fibromyalgia and patients with back pain. It is well known that cannabinoids (THC) accelerate learning processes. It is assumed that the combination of both treatments may exert an synergetic effect. A low dose of THC is used, which ist not expected to have direct analgetic effects. The study also investigates genetic determinants of both disorders and the response to treatment, respectively.
The patients will be randomly assigned to one of four groups: Behavioral therapy and Dronabinol, behavioral therapy and placebo, behavioral therapy only, standard medical therapy. Patients will attend 12 weekly group-sessions (6-8 patients) of behavioral therapy. Behavioral therapy sessions will include training in reducing pain behaviour and establishing active and "healthy" behaviour instead. There will be weekly medical safety visits, in which the patients receive medication and undergo a physical examination (blood and urine samples).
Patients will be evaluated before and after behavioral therapy and will be followed for an additional 6- and 12-months phase. The outcome variables will be recorded by the use of interviews and questionnaires.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Principal Investigator: | Justus Benrath, MD, PhD | University of Heidelberg |
More Information
| ClinicalTrials.gov Identifier: | NCT00176163 History of Changes |
| Other Study ID Numbers: | kfg107 |
| Study First Received: | September 13, 2005 |
| Last Updated: | February 1, 2010 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
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Fibromyalgia Back pain Behavior Therapy Operant learning Tetrahydrocannabinol |
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Back Pain Fibromyalgia Myofascial Pain Syndromes Pain Neurologic Manifestations Nervous System Diseases Signs and Symptoms Muscular Diseases Musculoskeletal Diseases Rheumatic Diseases Neuromuscular Diseases |
Tetrahydrocannabinol Hallucinogens Physiological Effects of Drugs Pharmacologic Actions Central Nervous System Agents Therapeutic Uses Psychotropic Drugs Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents |