A controlled study of fluvoxamine and exposure in obsessive-compulsive disorder
- PMID: 2110206
- DOI: 10.1097/00004850-199001000-00002
A controlled study of fluvoxamine and exposure in obsessive-compulsive disorder
Abstract
DSM-3 obsessive-compulsive out-patients were randomly assigned to fluvoxamine with antiexposure (F), fluvoxamine with exposure (Fe), or placebo with exposure (Pe) for 24 weeks. Of 65 patients offered treatment 60 entered the trial, 50 reached week 8, 44 completed treatment to week 24, and 37 reached follow up to week 48. On average the patient had depressed mood (mean Hamilton depression rating scale = 19). Drop-out numbers, clinical status and behavioural measures were comparable across groups. Most F patients did not do antiexposure, but Fe and Pe patients complied in doing exposure. All three groups improved in rituals and depression from week 0 to week 24 and 48, with a slight but non-significant superiority for combined treatment up to week 24. At week 8 there was a drug between-group effect on rituals, but not on depression. At week 24 there was a drug between-group effect on depression, but not on rituals. The drug superiority was short-lived. At week 48 there was no between-group difference in rituals or depression. Depression was related to ritual outcome at week 24 in F, and tended to be so in Fe.
Similar articles
-
Exposure therapy, fluvoxamine, or combination treatment in obsessive-compulsive disorder: one-year followup.Psychiatry Res. 1993 Oct;49(1):63-75. doi: 10.1016/0165-1781(93)90030-k. Psychiatry Res. 1993. PMID: 8140182 Clinical Trial.
-
Fluvoxamine treatment of obsessive-compulsive disorder.Am J Psychiatry. 1987 Dec;144(12):1543-8. doi: 10.1176/ajp.144.12.1543. Am J Psychiatry. 1987. PMID: 3120604 Clinical Trial.
-
Efficacy of fluvoxamine in obsessive-compulsive disorder. A double-blind comparison with placebo.Arch Gen Psychiatry. 1989 Jan;46(1):36-44. doi: 10.1001/archpsyc.1989.01810010038006. Arch Gen Psychiatry. 1989. PMID: 2491940 Clinical Trial.
-
Treatment of obsessive compulsive disorder: psychotherapies, drugs, and other somatic treatment.J Clin Psychiatry. 1990 Aug;51 Suppl:44-50; discussion 55-8. J Clin Psychiatry. 1990. PMID: 2116405 Review.
-
Fluvoxamine as an antiobsessional agent.Psychopharmacol Bull. 1989;25(1):31-5. Psychopharmacol Bull. 1989. PMID: 2505302 Review.
Cited by
-
Clinical advances in obsessive-compulsive disorder: a position statement by the International College of Obsessive-Compulsive Spectrum Disorders.Int Clin Psychopharmacol. 2020 Jul;35(4):173-193. doi: 10.1097/YIC.0000000000000314. Int Clin Psychopharmacol. 2020. PMID: 32433254 Free PMC article. Review.
-
Long-term harms from previous use of selective serotonin reuptake inhibitors: A systematic review.Int J Risk Saf Med. 2019;30(2):59-71. doi: 10.3233/JRS-180046. Int J Risk Saf Med. 2019. PMID: 30714974 Free PMC article.
-
Promoting OCD WEllness and resilience (POWER) study: Rationale, design, and methods.Psychiatry Res Commun. 2023 Jun;3(2):100111. doi: 10.1016/j.psycom.2023.100111. Epub 2023 Mar 11. Psychiatry Res Commun. 2023. PMID: 37377947 Free PMC article.
-
Selective serotonin reuptake inhibitors.BMJ. 1992 Jun 27;304(6843):1644-6. doi: 10.1136/bmj.304.6843.1644. BMJ. 1992. PMID: 1633513 Free PMC article. No abstract available.
-
A promising randomized trial of a new therapy for obsessive-compulsive disorder.Brain Behav. 2012 Jul;2(4):443-54. doi: 10.1002/brb3.67. Epub 2012 Jun 26. Brain Behav. 2012. PMID: 22950048 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical