Piai 1979.
Methods | RCT with cross‐over design | |
Participants | 18 patients Unclear setting Diagnostic criteria not defined 56% females |
|
Interventions | Spasmolytic prifinium 30 mg tds for 3 weeks | |
Outcomes | Global assessment, dichotomous | |
Notes | No run‐in | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Random number table |
Allocation concealment (selection bias) | Unclear risk | Not described |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Double‐blind, methods not described |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No drop‐outs |
Selective reporting (reporting bias) | Low risk | All expected outcomes are reported |
Other bias | Low risk | The study appears to be free of other sources of bias |