Clinical Trials Directory

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

TypeNameDescription
DRUGOralDiltiazem 0.25mg/kg injection, give over 2 minutes, max dose 30mg
DRUGIntravenous drugthese 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

Source: ClinicalTrials.gov record NCT05391893. Inclusion in this directory is not an endorsement.