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Comparing 10-day and 4-month doxycycline courses for treatment of Chlamydia trachomatis-reactive arthritis: a prospective, double-blind trial.

AbstractOBJECTIVE:
To compare the efficacy of a 10-day and a 4-month doxycylcine course for the treatment of Chlamydia trachomatis-reactive arthritis (Ct-ReA).
METHODS:
Patients with active Ct-ReA were enrolled in a prospective, multicentre, double-blind, controlled clinical trial and randomised to receive doxycycline 100 mg twice daily for 10 days followed either by placebo or by continued doxycycline 100 mg twice daily over 4 months. Various clinical and laboratory parameters referring to disease activity were recorded in the beginning and at the end of treatment.
RESULTS:
32 of 37 patients included (15 men and 17 women; mean (standard deviation) disease duration 17 (13) months completed the study; 17 were randomised to short-term doxycycline and placebo (placebo group) and 15 to prolonged treatment with doxycycline (doxycycline group) over the 4-month study period. After this time, only two patients from each group went into remission. There were no drop-outs owing to adverse events or treatment failures.
CONCLUSIONS:
The results of this study suggest that prolonged treatment with a 4-month course of doxycycline is not superior to short-term treatment over 10 days in patients with Ct-ReA.
AuthorsN Putschky, H-G Pott, J G Kuipers, H Zeidler, M Hammer, J Wollenhaupt
JournalAnnals of the rheumatic diseases (Ann Rheum Dis) Vol. 65 Issue 11 Pg. 1521-4 (Nov 2006) ISSN: 0003-4967 [Print] England
PMID17038453 (Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial)
Chemical References
  • Anti-Bacterial Agents
  • PHB2 protein, human
  • Prohibitins
  • Doxycycline
Topics
  • Adult
  • Anti-Bacterial Agents (administration & dosage, therapeutic use)
  • Arthritis, Reactive (drug therapy)
  • Chlamydia Infections (drug therapy)
  • Chlamydia trachomatis
  • Double-Blind Method
  • Doxycycline (administration & dosage, therapeutic use)
  • Drug Administration Schedule
  • Female
  • Humans
  • Male
  • Middle Aged
  • Prohibitins
  • Prospective Studies
  • Severity of Illness Index
  • Treatment Outcome

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