Effect of Pre-Hospital ARNI Therapy on Short-Term Outcomes in HFrEF
NCT ID: NCT07347925
Last Updated: 2026-01-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
140 participants
OBSERVATIONAL
2026-01-10
2026-05-01
Brief Summary
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The study will compare two groups of participants: those who were already taking ARNI before coming to the hospital and those who were not. Information will be collected from medical records during the hospital stay, including heart-related events, kidney-related events, and how long participants stay in the hospital.
Some participants will also be followed for a short period after discharge. This study may help improve understanding of outcomes associated with ARNI use in people with heart failure in routine clinical care.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Prehospital ARNI users
Prehospital ARNI use
Participants who were using ARNI therapy before hospital admission
Non-Prehospital ARNI users
No prehospital ARNI use
Participants who were not using ARNI therapy before hospital admission
Interventions
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Prehospital ARNI use
Participants who were using ARNI therapy before hospital admission
No prehospital ARNI use
Participants who were not using ARNI therapy before hospital admission
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Future University in Egypt
OTHER
Responsible Party
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Mrwan Ayman Ahmed Eassa
MS Student, Clinical Pharmacy Department, Future University in Egypt
Locations
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Mansoura university Hospital
Al Mansurah, , Egypt
Countries
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Facility Contacts
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Other Identifiers
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REC-FPFUE-NO3/2025
Identifier Type: -
Identifier Source: org_study_id
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