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Fluoxetine response: endpoint vs pattern analysis.

Abstract
A 6-week double-blind trial of fluoxetine treatment of unipolar major depressive disorder in 49 patients was evaluated in terms of improvement in the Hamilton Depression Rating Scale (HDRS) and Clinical Global Improvement (CGI) scores. A relationship was found between change in HDRS (absolute and percentage decrease from baseline) and final CGI ratings. However, because of a few placebo-responders, endpoint analysis with both the HDRS and CGI showed no differences between active drug and placebo. Pattern analysis of persistent response did successively separate active drug from placebo (less than 0.05).
AuthorsR R Fieve, P J Goodnick, E Peselow, A Schlegel
JournalInternational clinical psychopharmacology (Int Clin Psychopharmacol) Vol. 1 Issue 4 Pg. 320-3 (Oct 1986) ISSN: 0268-1315 [Print] England
PMID3549877 (Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Propylamines
  • Fluoxetine
Topics
  • Adolescent
  • Adult
  • Aged
  • Clinical Trials as Topic
  • Depressive Disorder (drug therapy)
  • Double-Blind Method
  • Female
  • Fluoxetine (therapeutic use)
  • Humans
  • Male
  • Middle Aged
  • Propylamines (therapeutic use)

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