Pre-hospital ARNI use and short-term outcomes in HFrEF

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study compares adults admitted with heart failure and left ventricular ejection fraction under 40% who were taking an angiotensin receptor–neprilysin inhibitor (sacubitril/valsartan) before hospital arrival to those who were not. Investigators will extract data from hospital records to record cardiac events, kidney-related events, length of stay, and selected short-term outcomes, with some participants followed briefly after discharge. No treatments are assigned as part of the study; analyses will adjust for baseline clinical differences to explore associations between pre-hospital ARNI use and outcomes. The work is conducted at a single center (Mansoura University Hospital) and reflects routine clinical care in that setting.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* \>= 18 years, male or female EF \<40%

Exclusion Criteria:

* EF\>40% Pregnancy or breastfeeding

Where it's running

• Mansoura university Hospital
  Al Mansurah, Egypt Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.