Medical Marijuana in the Pediatric Central Nervous System Tumor Population
NCT ID: NCT03052738
Last Updated: 2024-08-29
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
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COMPLETED
19 participants
OBSERVATIONAL
2016-01-15
2020-06-30
Brief Summary
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Detailed Description
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The Investigators will administer PedsQLTM questionnaires and diaries to gather data regarding use practices, method of delivery, strain used, dosing and frequency, and family financial impact on all enrolled patients. The Investigators will also collect peripheral blood samples to evaluate for evidence of immuno-modulation by cannabinoids in patients who may already be immunocompromised and to assess blood cannabinoid levels.
This study will provide novel exploratory data regarding use patterns, impact on families and resources, and potential clinical benefits and harms associated with the growing marijuana use in the pediatric neuro-oncology population. Such information may guide future children afflicted with CNS tumors and their families to make decisions about whether to pursue cannabinoid treatment.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Parents/legal guardian(s) that will be completing the questionnaires must sign consent. There are no age parameters for parent/legal guardians' participation on study.
3. Patients must have a diagnosis of central nervous system (brain or spinal) tumor
4. Patients must be ONE of the following:
* Undergoing disease-directed therapy or disease surveillance as prescribed by the Pediatric Neuro-Oncology physicians at CHCO
* Planning to transfer medical care to Pediatric Neuro-Oncology physicians at CHCO from outside facilities
* Receiving palliative care services that are managed in conjunction with physicians at CHCO
5. Interest in marijuana use has been discussed by the patient or parents.
6. Patient has not used any marijuana products or synthetics in the last 14 days (a washout period of 14 days is permitted for those interested in participating on this study)
1. An exception to this rule is if patients took their first dose within 72 hours of signing consent. These patients will be eligible for study without going through a washout period.
2. Use (or planned use) of synthetic marijuana products as sole cannabinoid therapy
2 Years
18 Years
ALL
No
Sponsors
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University of Colorado, Denver
OTHER
Responsible Party
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Principal Investigators
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Nicholas K Foreman, MD
Role: PRINCIPAL_INVESTIGATOR
University of Colorado, Denver
Locations
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Chilsdren's Hospital Colorado
Aurora, Colorado, United States
Countries
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Other Identifiers
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15-0404.cc
Identifier Type: -
Identifier Source: org_study_id
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