Phase
Condition
Lactation Insufficiency
Miscarriage
Treatment
Nicotinamide riboside chloride
Placebo
Clinical Study ID
Ages > 16 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
informed consent for participation of both mother and baby
infant delivered at ≤28 weeks gestation
Infant born at the UC Davis Medical Center or transferred to the UC Davis MedicalCenter NICU within the first 6 days of life.
Mothers willing to express and measure milk volume
Exclusion
Exclusion Criteria:
Infant is participating in an intervention trial that could influence growth,development, or feeding tolerance
Mother has previously undergone breast surgery or has experienced other breasttrauma
Mother is actively using narcotics or amphetamines
Mothers is receiving cancer treatment
Mothers is receiving lithium or gold therapies
Mother plans to use any form of galactagogue (including fenugreek)
Mother is taking any form of contraceptives or plans to resume use of contraceptivewithin four weeks of delivery
Mother is involuntarily confined
Mother is an adult unable to consent
Mother resides <50 miles from UC Davis Medical Center
Anyone deemed unfit for participation by investigator(s)
Study Design
Connect with a study center
UC Davis Department of Food Science and Technology
Sacramento, California 95817
United StatesActive - Recruiting
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