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Exploration of recombinant hypertonic saline combined with furosemide in the treatment of heart failure

The role of compound hypertonic salt solution in the treatment of heart failure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017270
Enrollment
Unknown
Registered
2018-07-20
Start date
2011-02-01
Completion date
Unknown
Last updated
2018-07-23

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

Conditions

heart failure

Interventions

1:C-HSS (100ml) combined with furosemide (40mg)
2:furosemide (40mg)

Sponsors

Cangzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. decompensated HF (dyspnoea, weakness, lower limb edema or anasarca) and chronic ischemic or non ischemic cardiomyopathy according to the definition of HF; Framingham criteria, and New York Heart Association functional classification for HF; 2. Be unresponsive to treatment with high doses of furosemide, spironolactone, angiotensin- converting enzyme (ACE) inhibitors, digitalis, and nitrates (reduction of urine volume, a constant increase of body weight (BW), and impairments caused by clinical HF as reported above, in spite of an increase in furosemide and a combination of other diuretics); 3. had started this therapy >6 months before hospitalization; and 4. left ventricular ejection fraction (EF) < 40%, serum creatinine (Scr) < 2 mg/dl, blood urea nitrogen (BUN) < 50 mg/dl, and urinary volume < 500 ml/day.

Exclusion criteria

Exclusion criteria: Exclusion criteria were age III or < III on admission or with NYHA class III at discharge; failure to follow the prescribed treatment; did not participate in scheduled clinical interviews, did not follow the prescribed diet, or serious water or activity restrictions.

Design outcomes

Primary

MeasureTime frame
survival;hospital stay,;readmission rate;mortality rate;diuretic resistance;the renin-angiotensin-aldosterone system (RAAS);

Countries

China

Contacts

Public ContactYanfang Wan

Cangzhou Central Hospital

wanyune2417@sina.com+86 13393276630

Outcome results

None listed

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