Short-Term Effects of Medicinal Cannabis Therapy on Spasticity in Multiple Sclerosis
NCT ID: NCT00248378
Last Updated: 2006-06-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE1/PHASE2
30 participants
INTERVENTIONAL
2001-09-30
2005-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
TREATMENT
DOUBLE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Smoked Cannabis
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Center for Medicinal Cannabis Research
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jody Corey-Bloom, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of California, San Diego
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
UC San Diego Medical Center
San Diego, California, United States
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Center for Medicinal Cannabis Research
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
030002
Identifier Type: -
Identifier Source: secondary_id
C00-SD-103
Identifier Type: -
Identifier Source: org_study_id