Duration of Marijuana Concentration in Breast Milk- A Pilot Study
NCT ID: NCT02635568
Last Updated: 2019-07-02
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
30 participants
OBSERVATIONAL
2016-11-30
2019-06-30
Brief Summary
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The specific aims are to determine in women who test positive for THC at delivery:
1. Determine length of time THC and metabolites are detected in breast milk of mothers who have a positive urine drug screen at the time of presentation for labor and delivery or within 72 hours of delivery.
2. Determine length of time THC and metabolites are detected in breast milk of mothers with postnatal exposure of either ingested or inhaled marijuana, to inform recommendations on when to safely return to breastfeeding.
3. Describe modes of marijuana consumption in women presenting for delivery and correlate with THC concentrations and persistence in breast milk.
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Detailed Description
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There are numerous documented benefits to breast milk, especially in preterm infants however sufficient literature exists to question the safety of THC's effects on the developing brain which may also be particularly susceptible in prematurity. Due to these unknown and understudied but highly concerning effects, The researchers faculty Neonatology practice has agreed to the consensus of refraining from knowingly administering breast milk from mothers actively using THC. Exemptions do occur in certain clinical settings. If this occurs during a mother's study enrollment, subsequent samples would be marked appropriately and the analytical data will be carefully examined.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Cannabis Use
Observational Study
Eligibility Criteria
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Inclusion Criteria
1. Standard of care urine toxicology screening at the time of delivery: Women who test positive for THC on a urine toxicology screening who intend to breastfeed will be recruited within 72 hours of delivery at University of Colorado Hospital (UCH) and mothers whose infants are admitted to Children's Hospital Colorado (CHCO) NICU.
2. Volunteers: Patients of UCH prenatal OB clinics, postpartum unit, and in the UCH and CHCO NICUs .
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Centers for Disease Control and Prevention
FED
University of Colorado, Denver
OTHER
Responsible Party
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Principal Investigators
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Erica Wymore, MD
Role: PRINCIPAL_INVESTIGATOR
Children's Hospital Colorado, University of Colorado Denver
Locations
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Children's Hospital Colorado
Aurora, Colorado, United States
University of Colorado Denver
Aurora, Colorado, United States
Countries
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Other Identifiers
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15-1639
Identifier Type: -
Identifier Source: org_study_id
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