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. 2018 Jun 28;2018(6):CD012721. doi: 10.1002/14651858.CD012721.pub2

Yuksek 2012.

Methods Study design: parallel, individual, RCT
Centres: 1, Turkey
Start of enrolment: May 2008
End of enrolment: March 2009
Mean follow‐up: 11 months
Run‐in period: not reported
Participants Inclusion criteria: "HF symptoms. They were ≥ 50 years old, had EF ≥ 50% and echocardiographic diastolic dysfunction."
Exclusion criteria: not reported
Randomised (N): 108 (54 intervention, 54 control)
Withdrawn (N): for reasons other than death 17 (not reported by arm)
Lost to follow‐up (N): 3 (not reported by arm)
Analysed (N): not reported
Age not reported
Sex not reported
Ethnicity not reported
Systolic blood pressure not reported
Heart rate not reported
BMI not reported
Serum creatinine not reported
B‐type natriuretic peptide not reported
NT pro B‐type natriuretic peptide not reported
LVEF not reported
NYHA class not reported
Hypertension not reported
Diabetes not reported
Atrial fibrillation not reported
Hospitalisation for heart failure: not reported
Coronary heart disease not reported
Stroke not reported
Diuretic not reported
Digoxin not reported
Beta‐blocker not reported
ACEI study drug
ARB not reported
MRA not reported
Interventions Intervention: perindopril, 10 mg/d
Comparator: "standard DHF treatment"
Concomitant medication: not reported
Outcomes Planned: we are not aware of a published protocol or a pre‐registration in a clinical trial register
Reported: T‐proBNP values and echocardiography
Notes no outcome data of interest
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk randomised, but no details
Allocation concealment (selection bias) Unclear risk not reported
Blinding of participants and personnel (performance bias) 
 All outcomes Unclear risk not reported
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk not reported
Incomplete outcome data (attrition bias) 
 All outcomes Unclear risk not reported
Selective reporting (reporting bias) Unclear risk unable to assess
Other bias Unclear risk funding not reported