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.
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Authors | S 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 |
Journal | The British journal of dermatology
(Br J Dermatol)
Vol. 117
Issue 1
Pg. 81-8
(Jul 1987)
ISSN: 0007-0963 [Print] England |
PMID | 3307890
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Chlorpheniramine
- Cimetidine
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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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