• 1 January 1979
    • journal article
    • research article
    • Vol. 11  (3) , 94-97
Abstract
To test the efficacy and toxicity of colloidal bismuth subcitrate (CBS) in a double-blind trial, 46 consecutive outpatients with active duodenal ulceration were randomly allocated to treatment with CBS or to a placebo for a period of 4 wk. Symptomatic assessment was based on frequency and severity of pain. The ulcer size was measured endoscopically before and at the end of the trial. During the trial blood and urinary bismuth [Bi] concentrations were measured. The symptomatic assessment of the patients receiving CBS or placebo showed that the reduction in pain was highly significant in both groups, but there was statistically significant difference in the degree of reduction of duodenal ulcer size in favor of the CBS-treated group (P < 0.025). A marked increase in urinary Bi concentration was noted, but the blood Bi levels remained within the acceptable levels.

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