BENITIONSClinical Trial Intelligence

Human Amniotic Membrane to Decrease Post Operative Atrial Fibrillation

Early Phase 1 Completed NCT04130061

ConditionAtrial Fibrillation
PhaseEarly Phase 1
SponsorUniversity of Utah
StatusCompleted
Enrollment27 participants
InterventionsHuman Amniotic Membrane
Start dateOct 11, 2019
Completion dateJun 1, 2021
Results postedDec 6, 2024

Summary

This study will evaluate the application of hAM at the time of cardiac surgery to decrease inflammation and the subsequent substrate to reduce incidence of post-operative atrial fibrillation. Patients will randomized 1:1 to receive either hAM application or standard of care.

Number of Participants With Adverse Events

1 month · Participants

Randomized0 Participants
Control0 Participants

Number of Participants With Post Op Atrial Fibrillation Between Patients Who Receive hAM and Controls

1 month · Participants

Randomized5 Participants
Control6 Participants

proBNP (Serum) Between Groups at Time of Surgery

Surgery · pg/mL

Randomized198 ± 263 pg/mL
Control347 ± 523 pg/mL

Open in BENITIONS View on ClinicalTrials.gov

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