Scholze 1999.
Methods | 2‐ to 4‐week single‐blind placebo run‐in; inclusion criteria= supine DBP 100‐115 mm Hg after run‐in; 6‐week double‐blind treatment | |
Participants | All patients: n=507(327 males,180 females); mean age=50.2 years; baseline SBP/DBP not reported | |
Interventions | Ramipril 2.5 mg once daily; Ramipril 5 mg once daily; Ramipril 10 mg once daily; Placebo | |
Outcomes | Mean change from baseline in trough supine SBP/DBP using mercury sphygmomanometer | |
Notes | BP change and SEM of change reported, endpoint BP and SD not reported; calculated SD of change from N and change SE; BP data from Table 1, p. 1453; Jadad score=3; funding source= Hoechst AG | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Unclear risk | B ‐ Unclear |