Methods | Country: Italy Setting/Design: University Time frame: NS Randomisation method: Yes Blinding ‐ Participants: No ‐ Investigators: No ‐ Outcome assessors: No ‐ Data analysis: No Intention‐to‐treat: Yes Follow‐up period: 6 months x 2 Loss to follow‐up: 0 | |
Participants |
Inclusion criteria
Enalapril group
Atenolol group
Exclusion criteria
|
|
Interventions |
Enalapril group
5 mg/d Atenolol group 50 mg/d Co‐interventions: NS |
|
Outcomes |
|
|
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Unclear risk | B ‐ Unclear |