Phase 4
Completed N=72
Efficacy and Safety of Galantamine for Improving Dysfunction in People With Bipolar Disorder
Source: ClinicalTrials.gov NCT00741598 ↗Enrolled (actual)
72
Serious AEs
0.0%
Results posted
May 2017
Primary outcomePrimary: Scores on the California Verbal Learning Test (CVLT-II) at Screening and Week 16 — 50.15; 47.21; 58.88; 52.90 number of total words remembered
◆ Published Evidence
No publication linked
No peer-reviewed publication reporting this trial's results has been linked yet. This can indicate results are unpublished — a known publication-bias signal. We re-check periodically.
Summary
This study will examine whether extended release galantamine, a drug approved by the Food and Drug Administration to reduce cognitive impairments in people with Alzheimer's disease, can perform the same function in stable people with bipolar disorder.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Scores on the California Verbal Learning Test (CVLT-II) at Screening and Week 16 |
50.15; 47.21; 58.88; 52.90 | — |
| PRIMARY Scores on the Wisconsin Card Sorting Test (WCST) at Screening and Week 16 |
45.87; 44.11; 29.70; 29.79; 51.94; 44.28 | — |
| PRIMARY The Conners' Continuous Performance Test (CPT) at Baseline, Weeks 4, 8, 12, and 16 |
22.16; 19.40; 21.87; 19.24; 15.61; 16.39 | — |
| SECONDARY The Range of Impaired Functioning Tool (LIFE-RIFT) |
10.39; 9.41; 9.66; 9.03; 9.07; 8.53 | — |
| SECONDARY Quality of Life Satisfaction Questionnaire (Q-LES-Q) |
62.3; 63.03; 66.03; 64.75; 62.62; 65.28 | — |
Eligibility Criteria
Inclusion Criteria
- DSM-IV diagnosis of Bipolar I disorder or Bipolar II disorder
- A baseline Hamilton-D 17 score of less than 10 at screening visit
- A baseline Young Mania Rating Scale (YMRS) score of less than 10 at screening visit
- No acute episodes of depression or mania for the previous 12 weeks
- Score of 17 or higher on the Massachusetts General Hospital (MGH) Cognitive and Physical Functioning Questionnaire
- Treated with psychiatric medications, alone or in combination, having only minimal, mild or moderate cognitive burden [as determined by a score of less than 3.5 on the MGH Cognitive Impact of Psychotropic Medications Scale (CIPMS).
- Able to understand English
Exclusion Criteria
- DSM-IV diagnosis of Bipolar NOS, Cyclothymia, or Schizoaffective Bipolar type.
- Meets DSM-IV criteria for acute manic, depressive, or mixed bipolar episode or had met full criteria for 2 consecutive weeks within the past 12 weeks prior to assessment
- Treated with psychiatric medications with large effects on cognition (as determined by a MGH Cognitive Impact of Psychotropic Medications Scale score of 4.0 or above)
- Pregnant women or women of child bearing potential who are not using a medically accepted means of contraception (defined as oral contraceptive pill or implant, condom, diaphragm, spermicide, IUD, s/p tubal ligation, partner with vasectomy)
- Serious suicide or homicide risk
- Unstable medical illness including cardiovascular, hepatic, renal, respiratory, endocrine, neurological, or hematological disease.
- History of seizure disorder, brain injury, or any known neurological disease (multiple sclerosis, degenerative disease such as ALS, Parkinson disease and any movement disorders, etc)
- The following DSM-IV diagnoses: 1) organic mental disorders; 2) any diagnosis of dementia; 3) substance use disorders, including alcohol, active within the last year; 4) schizophrenia; 5) delusional disorder; 6) psychotic disorders not elsewhere classified; 7) schizoaffective disorder; 8) major depressive disorder; 9) acute bereavement; 10) severe borderline or antisocial personality disorder
- Presence of mood congruent or mood incongruent psychotic features
- Clinical or laboratory evidence of hypothyroidism
- History of multiple adverse drug reactions, allergy to galantamine or other AChEIs
- Current use, or use within the last week, of excluded drugs (psychotropic medications and other central nervous system (CNS)-active drugs)
- Taken an investigational psychotropic drug within the last year
- Had electroconvulsive therapy (ECT) within the 6 months preceding enrollment
Data sourced from ClinicalTrials.gov (NCT00741598). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.