Clinical Trials Directory

Trials / Completed

CompletedNCT00720473

Lamotrigine Therapy in Geriatric Bipolar Depression

Lamotrigine Therapy in the Treatment of Geriatric Bipolar Depression: An Evaluation of Markers of Cerebral Energy Metabolism

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
69 (actual)
Sponsor
Mclean Hospital · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Accepted

Summary

We propose to study the efficacy and tolerability of lamotrigine in the treatment of older adults with bipolar depression and to compare measures of brain energy metabolism between older subjects with bipolar depression and healthy age-matched controls in order to better understand treatment response in geriatric bipolar depression.

Detailed description

We will use MRI techniques and neuropsychological testing to investigate potential markers of treatment response in elderly bipolar depressed patients receiving lamotrigine and age-matched, non-depressed controls. We intend to test these hypotheses: 1. At least 50% of older subjects with bipolar depression will respond treatment with lamotrigine as evidenced by a 50% reduction on the Montgomery Asberg Rating Scale (MADRS). In addition, treatment with lamotrigine will be safe and well tolerated as evidenced by a drop-out rate of less than 10% due to adverse effects. 2. Compared with healthy age-matched, non-demented, non-depressed controls, subjects with geriatric bipolar depression will demonstrate abnormalities in cerebral energy metabolism as assessed by elevated levels of glutamate and lactate, and decreased levels of NAA, using 1H MRS at 4T. 3. Successful treatment with lamotrigine in geriatric bipolar depression will result in decreases in lactate and glutamate, and elevations in NAA. 4. Baseline measures of executive functioning and information processing speed (measured by performance on the Wisconsin Card Sorting Test (WCST), Trails A and B and Stroop tests) will be impaired in subjects with geriatric bipolar depression compared with healthy controls. These measures will improve with successful treatment with lamotrigine and correlate with improvements in markers of cerebral energy metabolism (lactate, glutamate, NAA).

Conditions

Interventions

TypeNameDescription
DRUGLamotrigineLamotrigine with dosage range from 25 mg to 200 mg per day.

Timeline

Start date
2006-04-01
Primary completion
2011-07-01
Completion
2011-12-01
First posted
2008-07-22
Last updated
2017-02-01
Results posted
2016-07-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00720473. Inclusion in this directory is not an endorsement.