Effects of Electroconvulsive Therapy (ECT) in Bipolar Depression

Bipolar Disorder Clinical Trial

Official title:

A Study of the Acute and Chronic Effects of Electroconvulsive Therapy on Glutamatergic Neurotransmission in Bipolar Depression

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01557933
• Other study ID #: 2011-P-000693
• Status: Withdrawn
• Phase: N/A
• First received: March 9, 2012
• Last updated: November 28, 2012
• Start date: April 2011
• Est. completion date: July 2012

Study information

• Verified date: November 2012
• Source: Mclean Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

The primary purpose of this study is to use magnetic resonance spectroscopy (MRS) to measure the levels of several brain chemicals including, but not limited to, glutamate, glutamine, and N-acetylaspartate, before and after treatment with ECT. In addition to MRS, the investigators will use several other MRI techniques including structural MRI, resting state functional MRI (fMRI), and diffusion tensor imaging (DTI) to measure how the structure and function of the brain changes with ECT.

The investigators hypothesize that the Gln/Glu ratio is increased in the anterior cingulate cortex (ACC), but not the parieto-occipital cortex (POC), following the first ECT treatment.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: July 2012
• Est. primary completion date: July 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Male or female age 18-55

• Meets DSM-IV criteria for Bipolar Disorder Type I, II, or NOS with current episode depressed

• Has been scheduled to be evaluated by an ECT consultant from the McLean Hospital ECT service

• Current score of greater than or equal to 24 on the Montgomery-Asberg Depression Rating Scale (MADRS)

Exclusion Criteria:

• Unwillingness or inability to provide informed consent

• Lifetime history of schizophrenia

• DSM-IV diagnosis of alcohol or substance dependence, with the exception of nicotine dependence, within three months prior to screening

• Positive urine toxicology screen at screening (NOTE: Participants with a positive urine toxicology screen who are prescribed benzodiazepine, stimulant, or opiate medications by their physician will be permitted to enroll in the study as long as they do not meet abuse or dependence criteria for these substances)

• Female participants with a positive urine pregnancy test at screening

• Pregnancy. Females of childbearing potential must be using an effective contraceptive method (e.g., abstinence, prescription oral contraceptives, contraceptive injections, MRI-safe intrauterine device, double-barrier method, male partner sterilization)

• Any contraindications to having an MRI scan, including cardiac pacemakers, metal vascular clips or stents, artificial heart valves, certain kinds of prostheses, brain stimulator devices, implanted drug pumps, ear implants, eye implants or known metal fragments in eyes, exposure to shrapnel or metal filings (wounded in military combat, sheetmetal workers, welders, and others), transdermal drug delivery systems, and certain tattoos with metallic ink. NOTE: Participants will be screened for these conditions at screening, and will be required to fill out a standard MRI screening form at the Brain Imaging Center, which will be reviewed by an MRI technician prior to each MRI scan

• Scheduled to receive first ECT treatment on a Friday

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Bipolar Disorder

Intervention

Other:
• No interventions will be used
No interventions will be used

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Mclean Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Gln/Glu ratio following the first ECT treatment	The Gln/Glu ratio is examined in the anterior cingulate cortex (ACC) and the parieto-occipital cortex (POC) following the first ECT treatment.	Participants will undergo an MR scan within 24 hours of their first ECT treatment	No
Secondary	The Gln/Glu ratio following the sixth ECT treatment.	The Gln/Glu ratio is examined in both the ACC and POC following the sixth ECT treatment.	Participants will undergo an MR scan within 24 hours of their sixth ECT treatment, which is approximately two weeks after their first ECT treatment	No