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Double blind study of ispaghula in irritable bowel syndrome.

A Prior, P J Whorwell
CCT Gut 1987 153 цитирований
PubMed DOI
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Study Design

Тип исследования
Randomized Controlled Trial
Размер выборки
80
Популяция
IBS patients
Вмешательство
Double blind study of ispaghula in irritable bowel syndrome. None
Препарат сравнения
placebo
Первичный исход
pain
Направление эффекта
Mixed
Риск систематической ошибки
Low

Abstract

A double blind placebo controlled trial of ispaghula husk in 80 patients with irritable bowel syndrome is reported. Global assessment judged treatment to be satisfactory in 82% of patients receiving ispaghula and 53% of the placebo group (p less than 0.02). Bowel habit was unchanged in the placebo group, while constipation significantly improved in patients taking ispaghula (p = 0.026). Transit time decreased significantly in those taking ispaghula compared with placebo (p = 0.001), especially in patients with initially high transit times. Abdominal pain and bloating improved in both groups, with no significant differences between ispaghula and placebo. Four of the eight withdrawals on ispaghula and 10 of the 15 withdrawals on placebo were because of treatment failure. Ispaghula significantly improves overall well being in patients with irritable bowel syndrome, and in those with constipation favourably affects bowel habit and transit time.

Кратко

Ispaghula significantly improves overall well being in patients with irritable bowel syndrome, and in those with constipation favourably affects bowel habit and transit time.

Used In Evidence Reviews

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