z-logo
Premium
Clinical trial: phase 2 study of lubiprostone for irritable bowel syndrome with constipation
Author(s) -
JOHANSON J. F.,
DROSSMAN D. A.,
PANAS R.,
WAHLE A.,
UENO R.
Publication year - 2008
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/j.1365-2036.2008.03629.x
Subject(s) - lubiprostone , irritable bowel syndrome , medicine , constipation , gastroenterology , placebo , abdominal pain , adverse effect , nausea , chronic constipation , alternative medicine , pathology
Summary Background  Analyses of a trial in constipated patients indicated that lubiprostone may be an effective treatment for irritable bowel syndrome with constipation. Aim  To assess the efficacy and safety of three lubiprostone doses for irritable bowel syndrome with constipation. Methods  195 irritable bowel syndrome with constipation patients received daily doses of 16 [8 μg twice daily (b.d.)], 32 (16 μg b.d.) or 48 μg (24 μg b.d.) lubiprostone or placebo b.d. for 3 months. Gastrointestinal parameters were recorded in diaries daily by patients. Results  After 1 month, lubiprostone showed significantly greater improvements in mean abdominal discomfort/pain scores vs. placebo ( P  = 0.023). After 2 months, all lubiprostone groups showed significantly greater improvements in mean abdominal discomfort/pain scores ( P  ≤ 0.039). After 3 months of treatment, the improvement in each lubiprostone arm was greater than placebo, but the test for trend was no longer significant. Treatment with lubiprostone showed significantly higher rates of gastrointestinal adverse events ( P  = 0.020), especially diarrhoea and nausea. Conclusion  Lubiprostone significantly improved gastrointestinal symptoms of irritable bowel syndrome with constipation at all doses. Higher doses of lubiprostone, especially the 48 μg/day group, were associated with more gastrointestinal adverse events. From these data, the 16 μg/day dose demonstrated the optimal combination of efficacy and safety. These results warrant further study of lubiprostone for treatment of irritable bowel syndrome with constipation patients.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here