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Taking people in IndonesiaPhase 4

Single and Twice-daily Dosing of Ramipril on Renal Function in Chronic Kidney Disease Patients With Reduced Ejection Fraction Heart Failure

Key facts

Where
Kartasura, IndonesiaSee the site
Phase
Phase 4

Where in Indonesia

  • UNS HospitalKartasura, IndonesiaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Evi Liliek Wulandari
Trial code
NCT07259512
Record updated
10 December 2025
Original description
This study compares the effects of once-daily versus twice-daily ramipril dosing on renal function in chronic kidney disease (CKD) patients with heart failure with reduced ejection fraction (HFrEF). Outcomes include changes in plasma renin activity, malondialdehyde, interleukin-6, albuminuria, and cystatin C after 30 days of therapy.Read full original descriptionShow less

Comparative Effects of Single Versus Twice-Daily Ramipril Dosing on Renal Function in Patients With Chronic Kidney Disease and Heart Failure With Reduced Ejection Fraction: Evaluation of Plasma Renin Activity, Malondialdehyde, Interleukin-6, Albuminuria, and Cystatin C

This study compares the effects of once-daily versus twice-daily ramipril dosing on renal function in chronic kidney disease (CKD) patients with heart failure with reduced ejection fraction (HFrEF). Outcomes include changes in plasma renin activity, malondialdehyde, interleukin-6, albuminuria, and cystatin C after 30 days of therapy.

Inclusion: Female or Male with age >18 years old; Patients with a diagnosis of CKD stage 3-5 non-dialysis with low ejection fraction heart failure (ejection fraction < 40%).

Exclusion: Receiving hemodialysis therapy; Receiving sacubitril-valsartan therapy; Receiving ARB therapy; History of intolerance to ACE inhibitors; History of angioedema to ACE inhibitors; Refractory hyperkalemia; Pregnancy; Hypotension with blood pressure <90/60, or patients in shock.

ClinicalTrials.gov NCT07259512