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Study on the Treatment of Heart Failure with Abnormal Blood Pressure by YQFM (Freeze-Dried) for Injection

Study on the Treatment of Heart Failure with Abnormal Blood Pressure by YQFM for Injection (Freeze-Dried)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110042
Enrollment
Unknown
Registered
2025-09-29
Start date
2025-02-12
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Heart Failure

Interventions

The hypertension treatment group was given injectable YQFM (freeze-dried) treatment on the basis of conventional Western medical treatment.:On the basis of the standard treatment in the YQFM group, YQ
The hypopiesis treatment group was given injectable YQFM (freeze-dried) treatment on the basis of conventional Western medical treatment.:On the basis of the standard treatment in the YQFM group, YQFM
The hypertension control group was given conventional Western medical treatment.:None
The hypopiesis control group was given conventional Western medical treatment.:None

Sponsors

The Second Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-75 years old; 2. According to the 2024 Chinese Guidelines for the diagnosis and treatment of heart failure, the patients were diagnosed with HFrEF, HFimpEF, and HFmrEF, and met the TCM syndrome criteria; 3. concurrent hypertension (HP>=140/90 MMHG according to the 2023ESH Guidelines for the management of hypertension) or hypotension (systolic blood pressure < 90mmHg within 72 hours and maintained between 90 and 110mmHg for more than 12 hours after treatment with vasoactive drugs); 4. The subjects voluntarily participated and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have a history of allergy to any component of Yiqifumai; (2) patients with severe liver and kidney dysfunction (eGFR<=30ml/min/1.73m^2 or active nephropathy, serum aminotransferase or bilirubin =3 times the upper limit of the clinical reference value), other serious primary or mental diseases affecting life span or malignant tumors; 3. Patients with pregnancy, preparation or suspected pregnancy, abortion, lactation or delivery in the past 6 months; 4. Participating in other clinical investigators; 5. Using other traditional Chinese medicine at the same time; 6. Patients with severe hypotensive shock; 7. Investigators deemed it inappropriate for participants.

Design outcomes

Primary

MeasureTime frame
Improvement of cardiac function;

Secondary

MeasureTime frame
NT-proBNP level;Blood pressure changes before and after treatment;

Countries

China

Contacts

Public ContactWang Junnan

The Second Hospital of Jilin University

jdeywjn@163.com+86 431 8113 6002

Outcome results

None listed

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