Abstract
Oral formulations of 5-aminosalicylic acid (mesalazine) appear less toxic than sulphasalazine. We have therefore compared sulphasalazine, low dose mesalazine and high dose mesalazine in the treatment of mild to moderate relapse of ulcerative colitis. Sixty one patients (32 men, aged 20-78 years) were randomly allocated to sulphasalazine 2 g daily, mesalazine 800 mg daily, or mesalazine 2.4 g daily in a double blind, double dummy, four week trial. Groups were comparable for age, sex, extent of disease, and pretrial sulphasalazine intake. Four patients were unable to complete the study because of treatment failure (two taking sulphasalazine and two high dose mesalazine). A further two patients taking sulphasalazine developed side effects necessitating withdrawal. Within treatment comparisons revealed significant improvement of: sigmoidoscopic grade in the sulphasalazine group; rectal bleeding, sigmoidoscopic and histological grade in the low dose mesalazine group; stool frequency, rectal bleeding and sigmoidoscopic grade in the high dose mesalazine group. Greater improvement in rectal bleeding (p less than 0.05) and sigmoidoscopic appearances (p less than 0.05) occurred in patients taking high dose mesalazine than in those taking sulphasalazine. In two patients taking high dose mesalazine minor rises of plasma creatinine concentrations occurred, suggesting the need to monitor renal function.
MeSH Terms
Adult
Aged
Aminosalicylic Acids/administration & dosage,adverse effects,therapeutic use
Clinical Trials as Topic
Colitis, Ulcerative/drug therapy
Delayed-Action Preparations
Double-Blind Method
Drug Administration Schedule
Female
Humans
Male
Mesalamine
Middle Aged
Random Allocation
Recurrence
Sulfasalazine/administration & dosage,adverse effects,therapeutic use
Chemicals
Aminosalicylic Acids
Delayed-Action Preparations
Sulfasalazine
Mesalamine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Riley S A
Department of Medicine, University of Manchester Medical School, Hope Hospital, Salford.
Mani V
Goodman M J
Herd M E
Dutt S
Turnberg L A
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