Clinical TrialID 8006
Prevention of Post-OP AFib Using Combination of CardiaMend and Amiodarone
NCT05681182
Post Operative Atrial Fibrillation
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 8006
- Evidence Id
- 8006
- Core Evidence Id
- 8006
- Source Clinical Trial Id
- 8001
- Herb2 Clinical Trial Id
- HBCT008001
- Nct Id
- NCT05681182
- Title
- Prevention of Post-OP AFib Using Combination of CardiaMend and Amiodarone
- Status
- Completed
- Phase
- Phase 4
- Study Result
- No
- Study Condition
- Post Operative Atrial Fibrillation
- Study Type
- Interventional
- Study Design
- Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: PREVENTION
- Intervention
- COMBINATION_PRODUCT: CardiaMend with the Addition of Amiodarone
- Intervention Allocation
- Intervention Model
- Single_Group
- Intervention Mask
- Intervention Purpose
- Prevention
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 30
- Outcome Measure
- Post Operative Atrial Fibrillation, The patient have continuous ECG monitoring until discharge to evaluate for any evidence of atrial fibrillation or atrial flutter which lasts longer than one hour or if less than one hour, requires medical or procedural intervention, Through discharge, an average of 2 weeks
- Sponsor Collaborator
- WakeMed Health and Hospitals|Helios Cardio Inc
- Funded By
- OTHER
- Location
- WakeMed Health and Hospitals, Raleigh, North Carolina, 27610, United States
- Other Id
- 1937514
- Start Date
- 2023-01-20
- Primary Completion Date
- 2024-02-06
- Completion Date
- 2024-02-06
- First Posted
- 2023-01-12
- Results First Posted
- Last Update Posted
- 2024-02-22
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT05681182
- Title Cn
- Title En
- Prevention of Post-OP AFib Using Combination of CardiaMend and Amiodarone
- Bilingual Status
- semi_complete