A Study Testing Drug Combination for Heart Failure in Women Comparing Increased Doses to Standard Care
- Participants:Adults
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Perindopril is a chemically synthesised medicine that belongs to the class of drugs called ACE inhibitors.[1] It is already authorised as a medicine.[1] In the clinical trial registry, perindopril is listed as a comparator drug, meaning it is used as a reference treatment against which other approaches are compared.[1] The form of perindopril described in the registry is perindopril arginine, which is available as oral tablets.[2] Perindopril is also known by its international non-proprietary name, perindopril arginine.[2]
Perindopril belongs to the group of medicines called ACE inhibitors. ACE stands for angiotensin-converting enzyme. This enzyme plays a role in producing a substance that narrows blood vessels and raises blood pressure. By blocking this enzyme, perindopril helps blood vessels relax and widen, which can reduce the workload on the heart. In the heart failure trial, perindopril is used as part of a broader set of heart failure medicines known as guideline-directed medical therapy.[1]
Perindopril arginine is available as oral tablets.[2] In the clinical trial, perindopril is listed at doses of 4 mg and 8 mg.[1] The route of administration recorded in the registry is buccal use, although the product information describes the tablet as an oral form.[1][2]
One registered clinical trial includes perindopril as a comparator drug. The trial is a Phase 3 randomised study with 368 participants.[1] It is authorised and is being conducted in heart failure.[1] The study compares up-titration of guideline-directed medical therapy, including perindopril, against usual care in women with heart failure.[1] The primary outcome is all-cause mortality within one year, heart failure readmission, or worsening heart failure.[1] The trial also looks at quality of life, adherence to medication, and side effects.[1]
The sources provided do not give a list of side effects for perindopril. The clinical trial record mentions that side effects are among the outcomes assessed, but no specific side effects are described.[1]
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