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Cimetidine and chlorpheniramine in the treatment of chronic idiopathic urticaria: a multi-centre randomized double-blind study.

Abstract
One hundred and twenty patients with chronic idiopathic urticaria, who entered a study at five centres (Sheffield, London, Bristol, Cardiff and Leeds) were treated with therapeutic doses of the H1 antagonist chlorpheniramine for 6 weeks. Histamine H1 non-responders (40 patients) were entered into a double-blind study and received chlorpheniramine plus cimetidine 400 mg q.d.s. (21 patients) or chlorpheniramine plus placebo (19 patients) for a further 8 weeks. The most important response measure was the change from baseline of the total symptom score: an assessment of the number and duration of new weals and degree of itching. There was a statistically significant difference between the average response in the two treatment groups in favour of chlorpheniramine plus cimetidine after 4 and 8 weeks' treatment (P less than 0.05 and P less than 0.01, respectively). No significant side-effects related to treatment were noted.
AuthorsS S Bleehen, S E Thomas, M W Greaves, J Newton, C T Kennedy, F Hindley, R Marks, M Hazell, N R Rowell, G M Fairiss
JournalThe British journal of dermatology (Br J Dermatol) Vol. 117 Issue 1 Pg. 81-8 (Jul 1987) ISSN: 0007-0963 [Print] England
PMID3307890 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Chlorpheniramine
  • Cimetidine
Topics
  • Chlorpheniramine (adverse effects, therapeutic use)
  • Cimetidine (therapeutic use)
  • Clinical Trials as Topic
  • Double-Blind Method
  • Drug Therapy, Combination
  • Humans
  • Random Allocation
  • Skin (pathology)
  • Urticaria (drug therapy, pathology)

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