Uridine Adolescent Bipolar Depression Randomized Controlled Trial
Completed · Not applicable · Has a placebo group
Conditions studied: Bipolar Disorder, Bipolar Depression, Manic Depression
In brief
This is a randomized, double-blind, placebo-controlled study of the investigational drug uridine as a treatment for depressed adolescents with bipolar disorder (i.e. "bipolar depression"). Participants initially randomized to placebo who complete the 6-week protocol will be offered 6 months of open-label uridine treatment and follow-up. Participants initially randomized to uridine will be offered the open-label treatment as well.
Key facts
- Study ID
- NCT01805440
- Run by
- University of Utah
- People needed
- 62
- Starts
- 2013-08-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2018-03-12
Who can join
Age: 13 and older, up to 21. Sex: any. Healthy volunteers: accepted.
You may not qualify if…
- Participants must not meet DSM criteria for a primary psychotic disorder, a developmental disorder or substance use disorder.
- Participants must not be at high risk for suicidal or homicidal actions.
- Participants must not be pregnant or breastfeeding.
- Participants must not have a contraindication to magnetic resonance imaging (e.g. ferromagnetic implant, or claustrophobic anxiety).
- Incarcerated persons are excluded, because this study is not approved for Research Involving Prisoners.
Where it is running
- University of Utah — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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