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Short-Term Effects of Medicinal Cannabis Therapy on Spasticity in Multiple Sclerosis

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Smoked Cannabis
Sponsored by
Center for Medicinal Cannabis Research
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Multiple Sclerosis, Cannabis, Spasticity, Tolerability

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Clinically definite or probable, laboratory-supported MS Complaints of spasticity and at least moderate increase in tone as evidenced by a score of >= 2 on the Modified Ashworth Scale at either the elbow, hip, or knee If on disease-modifying therapy ("ABC"), have been on a stable dose for at least six months Fluent in English If not cannabis-naive, must refrain from smoking cannabis for two weeks prior to screening (confirmed by urinalysis) If on either lioresal (Baclofen) or tizanadine (Zanaflex), have been on a stable dose for at least three months >=18 years of age Exclusion Criteria: Axis I psychiatric disorder especially depression or significant neurological disease other than MS as determined by the PI Recent history of active substance abuse defined as daily use for at least 14 days within the past month Drug use restrictions, eg, subjects on probation or parole, employment involving high risk to themselves and/or the public (airline pilot, bus driver, etc.) Any unstable medical health problem Any known pulmonary disorders, including tuberculosis, asthma, or COPD Pregnant or nursing Require benzodiazepines to control spasticity Require high doses of analgesic medications on a daily basis

Sites / Locations

  • UC San Diego Medical Center

Outcomes

Primary Outcome Measures

Reduction in spasticity as indicated by the: Ashworth Spasticity Scale, Timed 25-ft Walk, and Grooved Pegboard Test

Secondary Outcome Measures

Tolerability of study drug as determined by the Brief Symptom Inventory, Subjective Ratings of High and Sedation-Revised, and UKU Side Effect Rating Scale
Effect of study drug on global functioning and quality of life as indicated by the Multiple Sclerosis Quality of Life Inventory

Full Information

First Posted
November 2, 2005
Last Updated
June 21, 2006
Sponsor
Center for Medicinal Cannabis Research
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1. Study Identification

Unique Protocol Identification Number
NCT00248378
Brief Title
Short-Term Effects of Medicinal Cannabis Therapy on Spasticity in Multiple Sclerosis
Official Title
Short-Term Effects of Medicinal Cannabis Therapy on Spasticity in Multiple Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2006
Overall Recruitment Status
Completed
Study Start Date
September 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Center for Medicinal Cannabis Research

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine whether or not smoked marijuana improves spasticity in patients with multiple sclerosis.
Detailed Description
Studies of cannabinoids for spasticity in MS have had mixed results but clinical studies have been small, generally not properly controlled, with results controversial, and difficult to interpret. Recently, investigators in the UK and US tested the ability of cannabinoids to control spasticity and tremor symptoms of the MS-like disease, experimental allergic encephalomyelitis, in mice (Baker et al, 2000). The authors found that four different cannabinoids quantitatively ameliorated both tremor and spasticity in diseased mice; thus providing rationale for patients' reports of the therapeutic effects of cannabis in the control of their MS symptoms. The present study will be a randomized, placebo-controlled, crossover design of 30 patients who will be assessed before and after treatment for 3 consecutive days (Phase I), undergo washout-out for a total of 11 days, and then cross over to either the placebo or active treatment phase (Phase II), depending on what they received during Phase I. At each study visit, patients will utilize a controlled puff procedure to help ensure stable intake (Levin et al, 1989). Comparisons: A single dose of 4% THC marijuana cigarette each day for 3 days will be compared to a placebo administered under the same dosing conditions for the relief of spasticity, drug tolerability, and changes in global functioning and quality of life indices.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple Sclerosis, Cannabis, Spasticity, Tolerability

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Smoked Cannabis
Primary Outcome Measure Information:
Title
Reduction in spasticity as indicated by the: Ashworth Spasticity Scale, Timed 25-ft Walk, and Grooved Pegboard Test
Secondary Outcome Measure Information:
Title
Tolerability of study drug as determined by the Brief Symptom Inventory, Subjective Ratings of High and Sedation-Revised, and UKU Side Effect Rating Scale
Title
Effect of study drug on global functioning and quality of life as indicated by the Multiple Sclerosis Quality of Life Inventory

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinically definite or probable, laboratory-supported MS Complaints of spasticity and at least moderate increase in tone as evidenced by a score of >= 2 on the Modified Ashworth Scale at either the elbow, hip, or knee If on disease-modifying therapy ("ABC"), have been on a stable dose for at least six months Fluent in English If not cannabis-naive, must refrain from smoking cannabis for two weeks prior to screening (confirmed by urinalysis) If on either lioresal (Baclofen) or tizanadine (Zanaflex), have been on a stable dose for at least three months >=18 years of age Exclusion Criteria: Axis I psychiatric disorder especially depression or significant neurological disease other than MS as determined by the PI Recent history of active substance abuse defined as daily use for at least 14 days within the past month Drug use restrictions, eg, subjects on probation or parole, employment involving high risk to themselves and/or the public (airline pilot, bus driver, etc.) Any unstable medical health problem Any known pulmonary disorders, including tuberculosis, asthma, or COPD Pregnant or nursing Require benzodiazepines to control spasticity Require high doses of analgesic medications on a daily basis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jody Corey-Bloom, M.D., Ph.D.
Organizational Affiliation
University of California, San Diego
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC San Diego Medical Center
City
San Diego
State/Province
California
ZIP/Postal Code
92093
Country
United States

12. IPD Sharing Statement

Links:
URL
http://cmcr.ucsd.edu
Description
Center for Medicinal Cannabis Research

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Short-Term Effects of Medicinal Cannabis Therapy on Spasticity in Multiple Sclerosis

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