Human Amniotic Membrane to Decrease Post Operative Atrial Fibrillation
Early Phase 1
Completed
NCT04130061
| Condition | Atrial Fibrillation |
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| Phase | Early Phase 1 |
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| Sponsor | University of Utah |
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| Status | Completed |
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| Enrollment | 27 participants |
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| Interventions | Human Amniotic Membrane |
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| Start date | Oct 11, 2019 |
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| Completion date | Jun 1, 2021 |
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| Results posted | Dec 6, 2024 |
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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
| Randomized | 0 Participants |
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| Control | 0 Participants |
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Number of Participants With Post Op Atrial Fibrillation Between Patients Who Receive hAM and Controls
1 month · Participants
| Randomized | 5 Participants |
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| Control | 6 Participants |
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proBNP (Serum) Between Groups at Time of Surgery
Surgery · pg/mL
| Randomized | 198 ± 263 pg/mL |
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| Control | 347 ± 523 pg/mL |
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Open in BENITIONS
View on ClinicalTrials.gov
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