Status:
COMPLETED
CoQ10 in Geriatric Bipolar Depression
Lead Sponsor:
Mclean Hospital
Collaborating Sponsors:
National Alliance for Research on Schizophrenia and Depression
Conditions:
Bipolar Depression
Eligibility:
All Genders
55-89 years
Phase:
NA
Brief Summary
We propose to study and compare measures of brain energy metabolism in geriatric bipolar individuals and healthy older adults. We would also like to investigate changes in brain energy metabolites and...
Detailed Description
Hypotheses 1. At baseline, the forward rate constant (kfor) of CK enzymatic activity in the frontal lobe of older subjects with bipolar depression will be significantly decreased relative to that of ...
Eligibility Criteria
Inclusion
- 55 years or older
- Meet DSM-IV diagnostic criteria for Bipolar Disorder, Current Episode Depressed
- Montgomery Asberg Depression Rating Scale (MADRS) Score of \>20
- If the MADRS score is \<20 but \>16, a diagnosis of bipolar disorder, current episode depressed, based on the Structured Clinical Interview of DSM IV TR (SCID) and Dr. Forester's initial interview would allow the subject to be included in the study.
- Young Mania Rating Scale (YMRS) Score of \< 6
- If the YMRS score is \>6 subjects can still be admitted if subjects do not meet clinical criteria for mania or hypomania at the time of screening
- Able to provide informed consent
- Must speak English
- Must be able to visit McLean Hospital for the screening visit and six study visits during the 8-week duration of the study
- Subjects may be taking other medications for bipolar depression including antidepressants, mood stabilizers and antipsychotic mediations prior to Co-Q10 therapy, but may not have any dosage adjustments of these medications in the week before Co-Q10 is added.
Exclusion
- Serious or unstable medical illness, including cardiovascular, hepatic, renal, respiratory, endocrine, neurologic or hematologic disease
- History of seizure disorder,
- History or current diagnosis of the following psychiatric illnesses: any organic mental disorder (including dementia), schizophrenia, schizoaffective disorder, delusional disorder, psychotic disorder not otherwise specified, unipolar major depressive disorder, patients with substance dependence disorders, including alcohol, active within the last 12 months.
- History of drug hypersensitivity or intolerance to Coenzyme Q10.
- Use of medications that are excluded in this study (barbiturates; however, the use of non-benzodiazepine sedative hypnotics (such as zolpidem (Ambien)) may be used as needed except within 12 hours of the MRI scan)
- Benzodiazepines may be used by subjects throughout the study as long as they are not taken within 12 hours of any MRI scan.
- Subjects diagnosed with a mitochondrial disorder.
- Subjects taking other putative mitochondrial enhancers (e.g., vitamin E, carnitine, creatine, Vitamin complex B, pramipexole) at the time of study entry.
- Any of the exclusion criteria mentioned in the MRI risks section below
Key Trial Info
Start Date :
July 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2010
Estimated Enrollment :
42 Patients enrolled
Trial Details
Trial ID
NCT00720369
Start Date
July 1 2008
End Date
March 1 2010
Last Update
January 13 2014
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
McLean Hospital
Belmont, Massachusetts, United States, 02478