Verapamil in affective disorders: a controlled, double-blind study
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu klinické zkoušky, srovnávací studie, klinické zkoušky kontrolované, časopisecké články
PubMed
2649156
DOI
10.1016/0006-3223(89)90157-1
PII: 0006-3223(89)90157-1
Knihovny.cz E-zdroje
- MeSH
- amitriptylin terapeutické užití MeSH
- bipolární porucha farmakoterapie MeSH
- depresivní poruchy farmakoterapie psychologie MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- klinické zkoušky jako téma MeSH
- lidé středního věku MeSH
- lidé MeSH
- náhodné rozdělení MeSH
- psychologické testy MeSH
- psychotické poruchy farmakoterapie MeSH
- úzkostné poruchy farmakoterapie MeSH
- verapamil terapeutické užití MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky kontrolované MeSH
- klinické zkoušky MeSH
- srovnávací studie MeSH
- Názvy látek
- amitriptylin 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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