NCT03840499UnknownNot Applicable
The Role of Willingness of Participation in Cardiology Trials on the Survival of Patients
Semmelweis University Heart and Vascular Center1 site in 1 country400 target enrollmentStarted: October 1, 2018Last updated:
Conditions
Interventions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 400
- Locations
- 1
- Primary Endpoint
- All-cause mortality
Study Overview
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.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 85 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Hospitalisation due to acute myocardial infarction, and or heart failure
- •Singed informed consent
Exclusion Criteria
- •Previous participation in any clinical study
- •Haemodinamically instable, shock, intubation
- •Pregnancy, breast feeding
Arms & Interventions
Willing to participate in clinical study
Intervention: Optimal medical therapy (Drug)
Not-willing to participate in clinical study
Intervention: Optimal medical therapy (Drug)
Outcomes
Primary Outcomes
All-cause mortality
Time Frame: 2-years
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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