Verapamil in affective disorders: a controlled, double-blind study
Language English Country United States Media print
Document type Clinical Trial, Comparative Study, Controlled Clinical Trial, Journal Article
PubMed
2649156
DOI
10.1016/0006-3223(89)90157-1
PII: 0006-3223(89)90157-1
Knihovny.cz E-resources
- MeSH
- Amitriptyline therapeutic use MeSH
- Bipolar Disorder drug therapy MeSH
- Depressive Disorder drug therapy psychology MeSH
- Adult MeSH
- Double-Blind Method MeSH
- Clinical Trials as Topic MeSH
- Middle Aged MeSH
- Humans MeSH
- Random Allocation MeSH
- Psychological Tests MeSH
- Psychotic Disorders drug therapy MeSH
- Anxiety Disorders drug therapy MeSH
- Verapamil therapeutic use MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Controlled Clinical Trial MeSH
- Clinical Trial MeSH
- Comparative Study MeSH
- Names of Substances
- Amitriptyline MeSH
- Verapamil MeSH
Eighty-six depressed inpatients were divided into four groups: patients in each of three groups were treated, respectively, with identical capsules of verapamil, amitriptyline, or placebo, whereas the fourth group was treated eclectically by the ward physician with so-called state-adjusted treatment (SAT). Each treatment period lasted 5 weeks. Psychopathology was assessed with the Hamilton Rating Scale for Depression, by the Zung self-rating scale, by the 100-mm analog scale, and by general clinical impression. Results indicated that amitriptyline and SAT were superior to verapamil or placebo. There was no significant difference between verapamil and placebo or between SAT and amitriptyline. This finding was more definitive in the homogeneous subgroup of 55 women with DSM-III diagnosis of Major depression. In addition, 12 manic inpatients (DSM-III) were treated orally with verapamil, 24 with neuroleptics, and 11 with both neuroleptics and lithium carbonate. The decline of their psychopathology, assessed by the Brief Psychiatric Rating Scale (BPRS) and general impression, was fully comparable. Using Analysis of Variance (ANOVA), the statistical difference among courses of psychopathology expressed as total BPRS scores reaches borderline significance in favor of verapamil. In contrast to neuroleptics, verapamil did not induce any sedative, hypnotic, or cataleptic effects, and was well tolerated.
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