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. 2011 Aug 10;2011(8):CD003460. doi: 10.1002/14651858.CD003460.pub3

Pulpeiro 2000.

Methods RCT
Participants 85 IBS patients
Hospital GI department
Mean age 45.2 years
69% female
Interventions Spasmolytic 
 Propinox 4 dd for 4 weeks
Outcomes Abdominal pain, continuous 
 Global assessment, dichotomous
Notes No run‐in
Dose unclear
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Not described
Allocation concealment (selection bias) Low risk Adequate
Blinding of participants and personnel (performance bias) 
 All outcomes Low risk Double‐blind, identical placebo
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No drop‐outs
Selective reporting (reporting bias) Low risk Expected outcomes reported
Other bias Low risk The study appears to be free of other sources of bias