A double-blind comparison of nefazodone,
imipramine, and placebo in major
depression
by
Fontaine R, Ontiveros A, Elie R, Kensler TT,
Roberts DL, Kaplita S, Ecker
JA, Faludi G
Louis-H. Lafontaine Hospital,
Research Centre, Montreal, Quebec, Canada.
J Clin Psychiatry 1994 Jun; 55(6):234-41
ABSTRACT
BACKGROUND: Nefazodone is a 5-HT2-receptor antagonist and serotonin (5-HT)
selective reuptake inhibitor. This study evaluates the safety and efficacy of
nefazodone in patients with major depressive disorder (MDD) in comparison to
imipramine and placebo treatments. It also compares two dose ranges of
nefazodone to investigate its optimal dose range. METHOD: Nefazodone was
evaluated in a 6-week, double-blind trial of novel design involving 180 patients
meeting Research Diagnostic Criteria for major depressive disorder and having a
minimum pretreatment score of 22 on the first 17 items of the Hamilton Rating
Scale for Depression (HAM-D). Patients were randomly assigned to placebo (2-10
capsules/day), imipramine (50-250 mg/day), or nefazodone in two dose ranges
(50-250 mg/day or 100-500 mg/day). RESULTS: Improvement on depression measures
with nefazodone in the 100-500-mg/day dose range (endpoint mean = 460 mg/day)
and imipramine (endpoint mean = 214 mg/day) exceeded that with placebo. Some
benefit was also observed in the nefazodone 50-250-mg/day treatment group
(endpoint mean = 242 mg/day), but it was suboptimal. Evidence of nefazodone's
efficacy as an antidepressant was consistently observed on physician- (HAM-D,
Clinical Global Impressions [CGI]) and patient-rated (CGI-patient rated) scales.
By patient self-report, improvement of anxiety symptoms associated with
depression was evident with nefazodone as early as the first week of treatment,
and benefit was seen with both nefazodone dosage groups. Analyses of the
physician's global assessments of therapeutic effect and side effects at end of
treatment showed therapeutic benefit for both nefazodone and imipramine
treatments; however, patients in the nefazodone treatment groups were
significantly less troubled by adverse experiences than were imipramine-treated
patients, resulting in a lower dropout rate for adverse experience. CONCLUSION:
Nefazodone is a well-tolerated and effective antidepressant for the treatment of
major depressive disorder.
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