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NCT01237379 · ClinicalTrials.gov registry record

Peroxisomal Defects and Familial Risk for Bipolar Disorder

A clinical trial, sponsored by University of Cincinnati.

Completed
Registry status
80
Enrollment target

NCT01237379 is a clinical trial that has completed, run by University of Cincinnati. The registered enrollment target is 80 participants.

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The verdict

NCT01237379 has completed, sponsored by University of Cincinnati.

COMPLETED
Registry status
80 participants
Enrollment target

Study Summary

The purpose of this study is to screen for peroxisome defects in child and adolescent offspring of Bipolar Disorder I (BD-I) parents at different stages of risk for transitioning to mania and following the onset of mania. Prediction 1: Youth with an elevated risk for developing BD-I and first-episode manic patients will exhibit graded deficits in measures of peroxisomal function compared with healthy controls. Prediction 2: Indices of peroxisomal function will be correlated with Red Blood Cells Docosahexaenoic acid (DHA) composition. Prediction 3: Graded deficits in measures of peroxisomal function will be inversely correlated with manic and depression symptom severity scores.

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2010-10
Est. Completion 2013-10

Sponsor

University of Cincinnati

245 total trials

What the Registry Record Tells You About NCT01237379

The ClinicalTrials.gov registry entry for NCT01237379 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Cincinnati, which has 245 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 0 interventions.

NCT01237379 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01237379 about?

NCT01237379 is a clinical study titled "Peroxisomal Defects and Familial Risk for Bipolar Disorder". The purpose of this study is to screen for peroxisome defects in child and adolescent offspring of Bipolar Disorder I (BD-I) parents at different stages of risk for transitioning to mania and following the onset of mania. Prediction 1: Youth with an elevated risk for developing BD-I and first-episo...

What is the current status of trial NCT01237379?

This trial is currently completed. The enrollment target is 80 participants. The study started on 2010-10. Estimated completion is 2013-10.

Who is sponsoring clinical trial NCT01237379?

This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.