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Clinical Trials/NCT00801567
NCT00801567
Withdrawn
Not Applicable

A Magnetic Resonance Spectroscopy Study of Change in Brain Bioenergetics in Bipolar Disorder in Response to Photic Stimulation

Mclean Hospital1 site in 1 countryJune 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bipolar Disorder
Sponsor
Mclean Hospital
Locations
1
Primary Endpoint
Change in brain levels of phosphocreatine (PCr), beta-nucleoside triphosphate (B-NTP), and intracellular pH (pHi).
Status
Withdrawn
Last Updated
14 years ago

Overview

Brief Summary

This study aims to gather additional information to support the theory that bipolar disorder is due to cellular (mitochondrial) dysfunction. To test this theory adults with bipolar disorder who are not currently symptomatic will receive a one-time brain scan (magnetic resonance spectroscopy [MRS] scan) with light stimulation. To test whether any MRS findings are specific to bipolar disorder, healthy controls and adults with schizophrenia will also be included in this study.

Detailed Description

This study will include males and females between the ages of 18 and 55 years. Participants will include adults with stable bipolar disorder or schizophrenia as well as healthy controls. The study involves a one-time visit that includes a clinical evaluation, laboratory tests, and a magnetic resonance scan that will last approximately 90 minutes. The procedures can also be separated into two study visits, if necessary.

Registry
clinicaltrials.gov
Start Date
June 2010
End Date
June 2010
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Brian P. Brennan, MD

Associate Director of Translational Neuroscience Research

Mclean Hospital

Eligibility Criteria

Inclusion Criteria

  • Male of female
  • 18-55 years
  • Bipolar, currently euthymic OR schizophrenia, stable, OR healthy control with no history of psychiatric illness
  • On stable medication with no changes in the two weeks prior to enrollment

Exclusion Criteria

  • History of substance abuse or dependence within 3 months of enrollment
  • Positive urine drug screen
  • Significant medical or neurological illness
  • Pregnancy
  • Any contraindication to magnetic resonance scanning, including claustrophobia

Outcomes

Primary Outcomes

Change in brain levels of phosphocreatine (PCr), beta-nucleoside triphosphate (B-NTP), and intracellular pH (pHi).

Time Frame: 42 minutes

Study Sites (1)

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