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Comparative study on the therapeutic effect of recombinant human brain natriuretic peptide for injection combined with vasoactive drugs on elderly patients with cardiac insufficiency and low blood pressure

Comparative study on the therapeutic effect of recombinant human brain natriuretic peptide for injection combined with vasoactive drugs on elderly patients with cardiac insufficiency and low blood pressure

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092788
Enrollment
Unknown
Registered
2024-11-22
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Cardiac insufficiency

Interventions

The recombinant human brain natriuretic peptide was pumped separately(0.0075µg/kg/min, adjusted according to blood pressure, no more than 3 days) :None
Recombinant human brain natriuretic peptide (0.0075µg/kg/min for 3 days) combined with metaraminol bitartrate injection (1-5mg/h, adjusted according to blood pressure):None
Recombinant human brain natriuretic peptide (0.0075µg/kg/min for 3 days) combined with dopamine hydrochloride injection (1-5µg/kg/min, adjusted according to blood pressure):None

Sponsors

Aerospace Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
80 Years to 100 Years

Inclusion criteria

Inclusion criteria: ? Age >= 80 years old ? Diagnosis of cardiac insufficiency (Framingham heart failure diagnostic criteria), with NYHA grade greater than Grade II. ? Meet the indication of using recombinant human brain natriuretic peptide. ? Basic systolic blood pressure at admission is 90-110mmHg. ? Voluntary participation and filling in the informed consent form (Ethics Committee of Aerospace Center Hospital)

Exclusion criteria

Exclusion criteria: ? Patients with cardiac insufficiency in non-clinical heart failure stage. ? Hemorrhagic shock ? Severe hepatic and renal insufficiency. ? Critical patients with unconsciousness and unstable vital signs. ? Patients who can't complete the treatment and observation due to the change of their condition or the change of the wishes of patients and their families.

Design outcomes

Primary

MeasureTime frame
BNP;

Secondary

MeasureTime frame
Data of cardiac color Doppler ultrasound;6-minute walking distance;MACE;

Countries

China

Contacts

Public ContactRui Meng

Aerospace Center Hospital

mengrui0711@163.com+86 158 1003 9867

Outcome results

None listed

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