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Qili Qiangxin capsule in management of chronic heart failure: A Randomized, double-blind, multi-center, placebo-controlled study

Integrative Medicine program optimization study in chronic heart failure

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003037
Enrollment
Unknown
Registered
2013-01-25
Start date
2013-01-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Heart Failure

Interventions

Qili Qiangxin capsule Group:Qili Qiangxin capsule + basal treatment (ACEI or ARB/ß-blockers/diuretics/with or without digoxin)
Placebo Group:Placebo+basal treatment (ACEI or ARB/ß-blockers/diuretics/with or without digoxin)

Sponsors

Shuguang hospital affiliated to Shanghai university of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Consistent with chronic heart failure diagnosis in patients with class II-III heart failure; The ages of 40-80 years old; heart-kidney yang deficiency syndrome; Willing to take Chinese medicine, and non-allergic.

Exclusion criteria

Exclusion criteria: Heart failure due to pericardial disease, arrhythmiaHeart failure caused due to non-cardiac causesHeart failure due to pulmonary embolism, or kidney, liver and other vital organs function failure; Associated with severe primary diseases of the liver, kidney and the endocrine, respiratory, hematopoietic system;Patients with severe infection, with advanced malignancies; the combined mental disorders and do not want to take Chinese medicine.

Design outcomes

Primary

MeasureTime frame
Cardiac function;TCM symptoms evaluation;Efficacy evaluation;Western medicine less stop rate;Cardiovascular all-cause mortality;Years of worsening heart failure number of admission;6-minute walk test;Quality of life survey;Echocardiography;BNP;Hypersensitivity CRP;Adverse events and adverse reactions;Safety Evaluation;

Countries

China

Contacts

Public ContactWang Xiaolong
wxlqy0214@163.com+86 13501991450

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026