Evaluation and Management of Heart Failure Patients
1 other identifier
observational
5,000
1 country
1
Brief Summary
The investigator is trying to improving our knowledge in the treatment of HF patients, for the purpose of improving their quality of life and reducing hospitalizations. For achieving this the investigator would like to build a registry which will include all the HF patients going an evaluation in the Heart Failure unit or clinic in our facility,
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2017
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
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 1, 2017
CompletedFirst Posted
Study publicly available on registry
May 5, 2017
CompletedStudy Start
First participant enrolled
July 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2031
February 2, 2022
February 1, 2022
13.5 years
May 1, 2017
February 1, 2022
Conditions
Outcome Measures
Primary Outcomes (2)
NP/ pro-BNP from baseline
10 years
QT measurements
ECG will be performed at baseline
10 years
Interventions
registry-no intervention After filling the informed consent the patients will be evaluated for clinical history and physical examination by the nurse and a cardiologist. Then, the patients may perform the following test: ECG, Chest X-RAY, Blood test including: complete blood count, renal and liver function, electrolytes, thyroid function, cholesterol, glucose, Troponin and Brain Natriuretic Peptide
Eligibility Criteria
Prospective registry which will include all the HF patients evaluated in the Heart Failure unit or clinic and will sign an informed consent form
You may qualify if:
- Age ≥18 years old
- Patient evaluated in the Heart Failure unit or clinic in our facility.
- Approved consent.
You may not qualify if:
- \. Patients who haven't signed the informed consent in the prospective group.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tel Aviv Medical Center
Tel Aviv, Israel
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michal Laufer Perl, MD
Tel Aviv Medical Center
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 10 Years
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of Research and development
Study Record Dates
First Submitted
May 1, 2017
First Posted
May 5, 2017
Study Start
July 1, 2017
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
December 31, 2031
Last Updated
February 2, 2022
Record last verified: 2022-02