Trials / Completed
CompletedNCT05391893
Effect of Oral and Intravenous Diltiazem Protocol for Emergency Department Atrial Fibrillation
Emergency Department Atrial Fibrillation Oral Diltiazem Observation Protocol
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 444 (actual)
- Sponsor
- Corewell Health South · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of the study is to reduce hospital admission and decrease time to disposition through establishing an effective treatment protocol for AF and Atrial Flutter in the Emergency Department of Spectrum Health Lakeland. Secondary outcome is to measure if oral diltiazem is an effective HR controlling agent in AF RVR and Flutter.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Oral | Diltiazem 0.25mg/kg injection, give over 2 minutes, max dose 30mg |
| DRUG | Intravenous drug | these patients will receive traditional treatments at provider discretion. They must receive at least one intravenous medication for atrial fibrillation with rapid ventricular response. This will be a heterogenous group of patients receiving digoxin, amiodarone, various beta-blockers, and intravenous diltiazem without oral diltiazem. |
Timeline
- Start date
- 2020-06-19
- Primary completion
- 2023-04-01
- Completion
- 2023-04-01
- First posted
- 2022-05-26
- Last updated
- 2024-12-27
- Results posted
- 2024-12-27
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05391893. Inclusion in this directory is not an endorsement.