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NCT06946095

Efficacy and Safety of Xinyue Capsule in the Treatment of Heart Failure With Preserved Ejection Fraction

Not yet recruiting Phase 3 Last updated 27 April 2025
What this trial tests

Phase 3 trial testing Chinese patent medicine in Heart Failure in 246 participants. Not yet recruiting.

Timeline
20 May 2025
Primary endpoint
31 October 2027
31 October 2027

Quick facts

Lead sponsorBeijing Anzhen Hospital
PhasePhase 3
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment246
Start date20 May 2025
Primary completion31 October 2027
Estimated completion31 October 2027

Drugs / interventions tested

Conditions studied

Sponsor

Beijing Anzhen Hospital

Who can join

18 and older, any sex, with Heart Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the effect of Xinyue Capsule in the improvement cardiac function and reduction the level of heart failure biomarker NT-proBNP in patients suffering from HF with an ejection fraction greater than or equal to 50%. Researchers will also collect information on how much the heart disease has impact on patient's lives, and how well Xinyue Capsule treatment is tolerated. The study plans to enroll 246 male and female patients of the age of 18 years and above suffering from heart failure with ejection fraction greater than or equal to 50%. Participants will take the study product as oral tablet with a dose 0.6 g Tid daily. Study duration will be up to 12 weeks.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Chinese patent medicine

Trials testing the same drug.

Other recruiting trials for Heart Failure

Currently open trials in the same condition.

Other Beijing Anzhen Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06946095.

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