Investigating a Tailored Diuretic Algorithm in Acute Heart Failure Patients
- Disease/Condition
- Heart Failure Acute
- Drug/Device/Intervention
- Urine sodium guided diuretic algorithm
- Study type
- Interventional
- Intervention type
- other
- Primary sponsor
- Zuyderland Medisch Centrum
- Location
- Heerlen, Netherlands
- Phase
- N/A
- Start date
- Feb 27, 2023
- End date
- Feb 27, 2026
- Enrollment
- 466 participants
Hierarchical composite of all-cause mortality, heart failure events and delta quality of life at 90 days follow-up.
Acutely decompensated heart failure (ADHF) is highly prevalent and has a high (financial)
 burden on the health care system. Treatment often consists of the administration of IV
 decongestive agents. Adequate dosing is difficult due to varying diuretic resistance and
 inadequate parameters to evaluate the response. Urine sodium is a promising biomarker to
 evaluate the diuretic response. It is hypothesized that a tailored, urine sodium guided
 diuretic algorithm will result in faster and more complete decongestion and therefore lead to
 better survival (in terms of mortality and heart failure events) while being non-inferior in
 terms of safety (mainly regression of kidney function).
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06092437
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06092437 through Pure Global AI's free database. This phase not specified trial is sponsored by Zuyderland Medisch Centrum and is currently Recruiting. The study focuses on Heart Failure Acute. Target enrollment is 466 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.