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The Effect of Bioelectrical Impedance Measurement Technology-Guided Diuretic Therapy on the Prognosis of Acute Decompensated Chronic Heart Failure

The Effect of Bioelectrical Impedance Measurement Technology-Guided Diuretic Therapy on the Prognosis of Acute Decompensated Chronic Heart Failure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111518
Enrollment
Unknown
Registered
2025-10-31
Start date
2025-12-12
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Heart failure

Interventions

Intervention Arm:Patients randomized within 24 hours of hospitalization underwent dry weight assessment exclusively based on BIA(Bioelectrical Impedance Analysis) measurements. Fluid status was evalua
values below -1.1L signaled over-diuresis, requiring reduction in diuretic intensity. Daily BCM measurements were obtained throughout hospitalization, with diuretic regimens adjusted in real-time base
Control Arm:The control arm received conventional decongestion therapy reflecting real-world practice patterns, where diuretic titration was guided by integrated assessment of clinical and laboratory

Sponsors

The First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. Hospitalization for acute decompensated heart failure or worsening heart failure symptoms; 3. Established prior diagnosis of chronic heart failure; 4. Clinical evidence of fluid overload (e.g., pulmonary rales, peripheral edema, jugular venous distension, ascites, pulmonary congestion, or radiographic pulmonary edema) requiring intravenous diuretic therapy as determined by the treating physician; 5. Provision of written informed consent

Exclusion criteria

Exclusion criteria: 1. Have other serious diseases that may endanger survival within 3 months, and have readmission plans (including revascularization, device implantation, etc.) within 3 months after discharge; 2. The history of two or more electrolyte disturbances in the past year; 3. Severe renal insufficiency (serum creatinine > 442µmol/L or eGFR < 30), nephrotic syndrome or receiving long-term regular dialysis; 4. Severe hypothyroidism and decompensated cirrhosis; 5. Lower extremity cellulitis, severe varicose veins, lymphedema, or deep vein thrombosis; 6. Pregnant or bedridden patients unable to take weight measurement; 7. Patients with fever or diarrhoea.

Design outcomes

Primary

MeasureTime frame
A composite endpoint of HF readmission and all-cause death within 3 months after discharge;

Secondary

MeasureTime frame
Re-hospitalized in March due to heart failure;Cardiovascular-related deaths in March;All cause death occurred in 3 months;The change of KCCQ quality of life score from baseline to discharge and 3 months after discharge;Dose of diuretics used during hospitalization;Dyspnea and changes in overall condition at 72 hours after admission (VAS scale);The incidence of hypotension during hospitalization;The incidence of electrolyte imbalance during hospitalization and follow-up period;Incidence of acute kidney injury during hospitalization;

Countries

China

Contacts

Public ContactLu Yanmei

The First Affiliated Hospital of Xinjiang Medical University

511026463@qq.com+86 189 0991 7855

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 9, 2026