The Role of Molecules in Blood Cells for Diagnosing Bipolar Disorders

Status Terminated

Clinical Trial Summary

The goal of this project is to study ~45 molecules in blood cells that may differentiate patients with bipolar disorder from healthy controls.

Clinical Trial Description

There is one study visit for this research protocol. Participants may complete this visit on the day that they sign consent. If there is an upcoming blood draw already scheduled for the participant, within the clinical research trial in which they are enrolled, they may decide to wait until then to receive their blood draw. In addition, if a subject has completed the protocol specific monitoring labs within the past 30 days, either for clinical or research purposes, they do not have to be repeated.

After obtaining the informed consent, all potential research participants will be assessed with a systemic clinical interview and a structured interview with the Mini-International Neuropsychiatric Interview (MINI). Psychiatric assessments will be administered to all participants, both healthy controls and participants diagnosed with bipolar disorder (BD). All eligible participants will also complete a Clinical Record Form. The form includes demographics, previous treatment history, the number of previous episodes, family history, and other historical correlates. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02804334
Study type	Observational
Source	University Hospitals Cleveland Medical Center
Contact
Status	Terminated
Phase
Start date	June 2016
Completion date	October 2018

View Details

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