Cardio-vascular Energy Transfer and Ventriculo-arterial Coupling in Heart Failure
1 other identifier
observational
30
1 country
1
Brief Summary
The goal of this pilot study is to investigate energy transfer fram the ventricle to the arteries in patients with heart failure, primary by investigating the total power.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Oct 2022
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2023
CompletedFirst Submitted
Initial submission to the registry
December 28, 2023
CompletedFirst Posted
Study publicly available on registry
January 10, 2024
CompletedJanuary 10, 2024
December 1, 2023
9 months
December 28, 2023
December 28, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Cardio vascular energy transfer in heart failure patients.
We are investigating cardio vascular energy transfer in heart failure patients by calculating total power.
During first 1-3 days after admission to hospital because of decompensated heart failure.
Eligibility Criteria
The study population comprises individuals experiencing decompensated heart failure within the first three days of hospital admission. It includes both newly diagnosed cases and individuals with a pre-existing heart failure diagnosis. The population is diverse, both regarding gender and etiology.
You may qualify if:
- Acute left ventricular failure due to:
- Myocardial ischemia
- Cardiomyopathy
- Myocarditis Sinus rhythm Age \>18 years
You may not qualify if:
- Cardiogenic shock Mechanical circulatory support Respiratory treatment Inotropic infusions Tachyarrhythmias Lack of capacity to consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- St. Olavs Hospitallead
- National Taiwan Normal Universitycollaborator
Study Sites (1)
St Olav hospital
Trondheim, Norway
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 28, 2023
First Posted
January 10, 2024
Study Start
October 1, 2022
Primary Completion
July 1, 2023
Study Completion
July 1, 2023
Last Updated
January 10, 2024
Record last verified: 2023-12