Clinical Trials Directory

Trials / Completed

CompletedNCT02697448

Comparison of Propofol and Sevoflurane as a Primary Anesthetic for Cardiac Ablation of Atrial Fibrillation.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
135 (actual)
Sponsor
Medical University of South Carolina · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Comparison of propofol and sevoflurane as a primary anesthetic for cardiac ablation of atrial fibrillation

Detailed description

A side effect of some volatile anesthetics, such as isoflurane and desflurane, is enhanced automaticity, accounting for secondary atrial pacemakers. Volatile anesthetics also have varying effects on the AV node and His-Pukinje system. These agents also prolong the QT interval and, for this reason, volatile anesthetics as a group have at times been avoided for atrial fibrillation ablation due to the fear that they may affect the efficacy of the ablation and increase recurrence. However, sevoflurane does not have the effects shown for other volatile anesthetics cardiac conduction. At this point there has not been a study comparing propofol, a non volatile anesthetic typically used in these cases, to sevoflurane, a volatile anesthetic, to determine if volatile anesthetics should be avoided during these procedures. This study will challenge the existing belief that sevoflurane increases the length of time to ablate atrial fibrillation and also decreases the efficacy of the ablation.

Conditions

Interventions

TypeNameDescription
DRUGpropofolParticipant receives propofol as anesthetic for cardiac ablation.
DRUGsevofluraneParticipant receives sevoflurane as anesthetic for cardiac ablations.

Timeline

Start date
2016-06-08
Primary completion
2023-06-30
Completion
2024-02-28
First posted
2016-03-03
Last updated
2024-08-20
Results posted
2024-08-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02697448. Inclusion in this directory is not an endorsement.