Abstract | BACKGROUND: METHODS: This was a randomized, double-blind, placebo-controlled, parallel group pilot trial with imipramine (50 mg) and citalopram (40 mg). RESULTS: Of 51 IBS patients randomized, baseline characteristics were comparable among the treatment arms; the majority was diarrhea-predominant. Adequate relief of IBS symptoms (primary endpoint) was similar for each treatment arm. Improvements in bowel symptom severity rating for interference (P = 0.05) and distress (P = 0.02) were greater with imipramine versus placebo, but improvements in abdominal pain were not. There was a greater improvement in depression score (P = 0.08) and in the SF-36 Mental Component Score (P = 0.07), with imipramine. Citalopram was not superior to placebo. Approximately 20% of the variance in scores was explained by treatment differences for abdominal pain, bowel symptom severity disability, depression and the mental component of the SF-36. CONCLUSION:
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Authors | Nicholas J Talley, John E Kellow, Philip Boyce, Christopher Tennant, Sandy Huskic, Michael Jones |
Journal | Digestive diseases and sciences
(Dig Dis Sci)
Vol. 53
Issue 1
Pg. 108-15
(Jan 2008)
ISSN: 0163-2116 [Print] United States |
PMID | 17503182
(Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antidepressive Agents, Second-Generation
- Antidepressive Agents, Tricyclic
- Citalopram
- Imipramine
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Topics |
- Adult
- Antidepressive Agents, Second-Generation
(therapeutic use)
- Antidepressive Agents, Tricyclic
(therapeutic use)
- Citalopram
(therapeutic use)
- Double-Blind Method
- Female
- Follow-Up Studies
- Humans
- Imipramine
(therapeutic use)
- Irritable Bowel Syndrome
(drug therapy)
- Male
- Patient Satisfaction
- Pilot Projects
- Prospective Studies
- Treatment Outcome
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