The Role of Willingness of Participation in Cardiology Trials on the Survival of Patients
1 other identifier
observational
400
1 country
1
Brief Summary
It has been shown retrospectively that participation and even the willingness improves the survival of patients after myocardial infarction or heart failure. We aimed to prospectively analyse the role of participation in cardiology trials on the survival of patients in a high volumen tertiary center.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2018
Longer than P75 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, 2018
CompletedFirst Submitted
Initial submission to the registry
February 12, 2019
CompletedFirst Posted
Study publicly available on registry
February 15, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2022
CompletedFebruary 15, 2019
February 1, 2019
4.3 years
February 12, 2019
February 12, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
All-cause mortality
2-years
Study Arms (2)
Willing to participate in clinical study
Not-willing to participate in clinical study
Interventions
Optimal medical therapy
Eligibility Criteria
Eligible subjects hospitalised due to myocardial infarction and or heart failure.
You may qualify if:
- Hospitalisation due to acute myocardial infarction, and or heart failure
- Singed informed consent
You may not qualify if:
- Previous participation in any clinical study
- Haemodinamically instable, shock, intubation
- Pregnancy, breast feeding
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Semmelweis University, Heart and Vascular Center
Budapest, 1122, Hungary
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 2 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 12, 2019
First Posted
February 15, 2019
Study Start
October 1, 2018
Primary Completion
December 31, 2022
Study Completion
December 31, 2022
Last Updated
February 15, 2019
Record last verified: 2019-02
Data Sharing
- IPD Sharing
- Will not share