A randomized, double-blind, placebo-controlled, phase 3 trial to evaluate the efficacy, safety, and tolerability of prucalopride in men with chronic constipation
Language English Country United States Media print-electronic
Document type Clinical Trial, Phase III, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
PubMed
25869393
PubMed Central
PMC4424376
DOI
10.1038/ajg.2015.115
PII: ajg2015115
Knihovny.cz E-resources
- MeSH
- Serotonin 5-HT4 Receptor Agonists adverse effects therapeutic use MeSH
- Benzofurans adverse effects therapeutic use MeSH
- Abdominal Pain chemically induced MeSH
- Headache chemically induced MeSH
- Medical Records MeSH
- Chronic Disease MeSH
- Defecation MeSH
- Adult MeSH
- Double-Blind Method MeSH
- Quality of Life MeSH
- Middle Aged MeSH
- Humans MeSH
- Nausea chemically induced MeSH
- Diarrhea chemically induced MeSH
- Surveys and Questionnaires MeSH
- Aged MeSH
- Severity of Illness Index MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase III MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Names of Substances
- Serotonin 5-HT4 Receptor Agonists MeSH
- Benzofurans MeSH
- prucalopride MeSH Browser
OBJECTIVES: Prucalopride is effective at alleviating symptoms of chronic constipation in women. The aim of this study was to assess the efficacy of 12 weeks of prucalopride treatment compared with placebo in men with chronic constipation. METHODS: This was a multicenter, stratified, randomized, parallel-group, double-blind, placebo-controlled, phase 3 study (ClinicalTrials.gov identifier: NCT01147926). The primary end point was the proportion of patients with a mean of three or more spontaneous complete bowel movements (SCBMs) per week across the treatment period. Efficacy end points were assessed using daily electronic diaries, global assessment of the severity of constipation and efficacy of treatment, and Patient Assessment of Constipation-Symptoms (PAC-SYM) and Patient Assessment of Constipation-Quality of Life (PAC-QOL) questionnaires. RESULTS: In total, 374 patients were enrolled in the study. Significantly more patients achieved a mean of three or more SCBMs per week in the prucalopride group (37.9%) than in the placebo group (17.7%, P<0.0001). The proportion of patients rating their constipation treatment as "quite a bit" to "extremely" effective at the final on-treatment visit was 46.7 and 30.4% in the prucalopride and placebo groups, respectively. The difference between treatment groups was statistically significant (P<0.0001). The proportion of patients with an improvement of at least 1 point in PAC-QOL satisfaction subscale score was 52.7 and 38.8% in the prucalopride and placebo groups, respectively (P=0.0035). Prucalopride had a good safety profile and was well tolerated. CONCLUSIONS: Prucalopride is effective, has a good safety profile, and is well tolerated for the treatment of men with chronic constipation.
Cliniques Universitaires Saint Luc Université Catholique de Louvain Brussels Belgium
Department of Gastroenterology County Durham and Darlington NHS Foundation Trust Durham UK
Institute of Rural Health Lublin Poland
Klinik fìr Gastroenterologie und Hepatologie Klinikum St Georg Leipzig Germany
Orlickoústecká nemocnice Ústí nad Orlicí Czech Republic
Shire Movetis NV Turnhout Belgium
Université Paris 5 René Descartes Paris France
University of Medicine and Pharmacy Carol Davila Bucharest Romania
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ClinicalTrials.gov
NCT01147926