The Kinocardiograph for assessment of fluid status in patients with heart failure

Completed

• Conditions: Heart failure (regardless of type and etiology)

• Registration Number: NL-OMON26847
• Lead Sponsor: Máxima Medical Centre, Eindhoven/Veldhoven, The Netherlands

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 15

Inclusion Criteria

1. Patients diagnosed with HFrEF, HFmrEF or HFpEF regardless of etiology
2. Presentation on the emergency department with ADHF
3. Age = 16 years
4. Able to speak and read the Dutch language

Exclusion Criteria

1. Atrial heart rhythm disturbances at presentation
2. Hemodynamic significant valvular disease
3. Pulmonary arterial hypertension due to other causes than a left sided heart problem
4. Receiving iv inotropic medication during hospital admission.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome is the correlation between changes in KE (mJ/heartbeat) and changes in fluid status (based on diameter and percentage collapse of the IVC).