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Life sciences · Phase 2 Trial
ClinicalTrials.gov · October 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 2 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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Registry record from ClinicalTrials.gov (NCT04944706). This is a study registration, not published results. Lead sponsor: Tasly Pharmaceutical Group Co., Ltd. Recruitment status: COMPLETED. Phase: PHASE2. Study type: INTERVENTIONAL. Enrollment: 225 participants (ACTUAL). Conditions: Chronic Heart Failure With Preserved Ejection Fraction. Interventions: DRUG: Qishen Yiqi dripping pills 2 bags/time + Qishen Yiqi dripping pills placebo 2 bags/time; DRUG: Qishen Yiqi dripping pills 4 bags/time; DRUG: Qishen Yiqi dripping pills placebo 4 bags/time. Primary outcome measures: 6-Minutes-Walking-Test (6MWT) , Baseline to weeks 12 and 24. Brief summary: Main objective: To evaluate the efficacy, safety and clinical dose exploration of Qishen Yiqi dripping pills in the treatment of chronic heart failure with preserved ejection fraction.