Ireland
--:--IST
Recruiting Observational

Evaluation and Management of Heart Failure Patients

NCT03142659 · tracked via the Priya Life Science Israel tracker
Phase
Observational
Started
2017-07-01
Last updated
2022-02-02

Condition(s) studied

Heart Failure

Investigational drug(s) / intervention(s)

registry-no intervention

registry-no intervention: 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

Study 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,

Eligibility

Sex
ALL
Min age
18 Years
Max age
120 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥18 years old 2. Patient evaluated in the Heart Failure unit or clinic in our facility. 3. Approved consent. Exclusion Criteria: 1\. Patients who haven't signed the informed consent in the prospective group.

Primary outcome measure(s)

  • NP/ pro-BNP from baseline — 10 years
  • QT measurements — 10 years
    ECG will be performed at baseline

Trial sites (1)

FacilityCityRegionStatus
Tel Aviv Medical Center Tel Aviv Israel Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03142659 on ClinicalTrials.gov ↗ ← All trials in Israel