In this retrospective cohort study, we plan to examine the relationship between buprenorphine
dose adjustments, gestational age, urine buprenorphine levels and the rate of neonatal
abstinence syndrome in opioid-maintained pregnant women
Other: Dose adjustments
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Full eligibility criteria for NCT03028883
Ages eligible for Study
14 Years to 55 Years
Genders eligible for Study
Accepts Healthy Volunteers
being treated at same location
All locations for NCT03028883
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Tris trial is registered with FDA with number: NCT03028883. The sponsor of the trial is St. Louis University and it is looking for 40 volunteers for the current phase.
Official trial title: Relationship Between Buprenorphine Dose Adjustments and Gestational Age in the Treatment of Opioid-Maintained Pregnant Women
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