Menu
Recruiting NCT06006819

Prognostic Markers of Acute Heart Failure With Chronic Kidney Disease

Observational Chronic Kidney Diseases Acute Heart Failure Biomarker

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Chronic Kidney Diseases, Acute Heart Failure, Biomarker. Basic parameters: 20 years — 90 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Plasma Proteomic Signature and the Prognosis of Acute Heart Failure With or Without Chronic Kidney Disease

Overview

Acute heart failure (AHF) is defined as new or worsening of symptoms and signs of heart failure and is the most frequent cause of unplanned hospital admission in elderly patients. N-terminal pro-brain natriuretic peptide (NT-pro-BNP) is one of the most developed prognostic markers for AHR patients and. NT-pro-BNP has limitations in terms of diagnostic or predictive accuracy in patients with chronic kidney disease (CKD). Plasma proteomics have the potential to examine underlying pathophysiological and prognostic roles, so we compared the plasma proteomic signature to predict outcomes of patients with or without CKD hospitalized for AHF.

Primary outcome measures

  • major adverse cardiovascular events [Time frame: 1 year]
Secondary outcome measures (1)
  • major adverse kidney events [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • hospitalized for acute heart failure

Exclusion criteria

  • initial serum NT-proBNP level <300ng/ml, pregnancy, amputated, and end-stage renal disease under regular dialysis

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Taiwan · 1 center
  • Cheng Hsin General Hospital — Taipei

Identifiers

NCT: NCT06006819 · CHGH(983)111A-61

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗