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Active Not RecruitingNCT03349528

Probiotics to Prevent Relapse After Hospitalization for Bipolar Depression

A Double-Blind Placebo-Controlled Trial of a Probiotic Supplement to Prevent Relapse and Improve the Clinical Course After Hospitalization for Bipolar Depression

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Sheppard Pratt Health System · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if taking a probiotic supplement versus a placebo will reduce relapse and improve the clinical course among participants who have been hospitalized for bipolar depression.

Conditions

Interventions

TypeNameDescription
BIOLOGICALProbiotic SupplementProbiotic supplement 1 tablet by mouth daily
BIOLOGICALInert CompoundProbiotic identical placebo 1 tablet by mouth daily

Timeline

Start date
2018-12-11
Primary completion
2026-12-01
Completion
2027-12-01
First posted
2017-11-21
Last updated
2026-04-07

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03349528. Inclusion in this directory is not an endorsement.

Probiotics to Prevent Relapse After Hospitalization for Bipolar Depression (NCT03349528) · Clinical Trials Directory