drugset / Trial / NCT05387967
Safety and Tolerability of Sacubitril/Valsartan in Heart Failure Patient With Reduced Ejection Fraction
NaSingle-groupOpen-labelTreatment
Summary
This proof-of-concept, open-label non-randomized clinical trial was conducted at a tertiary care cardiac center in Karachi, Pakistan. Patients with HFrEF were prescribed Sacubitril/Valsartan and followed for 12 weeks for the assessment of safety and tolerability. Safety measures included incidence of hypotension, renal dysfunction, hyperkalemia, and angioedema
Timeline
- Start
- 2021-01-01
- Primary completion
- 2021-06-30
- Completion
- 2021-09-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Sacubitril | Small molecule | 97 mg | — |
| Subject | Sacubitril | Small molecule | 100 mg | — |
| Subject | Valsartan | Small molecule | 103 mg | — |
| Subject | Valsartan | Small molecule | 200 mg | — |