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UnknownNCT02825498

Randomised Prospective Trial Comparing Contact Force and Non-contact Force Guided Catheter Ablation for Cavotricuspid Isthmus Dependent Atrial Flutter

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Victoria Cardiac Arrhythmia Trials · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Radiofrequency ablation (RFA) is a standard treatment option for cavotricuspid isthmus (CTI) dependent atrial flutter. We plan to perform a randomized prospective trial comparing the efficacy of contact force (CF) guided CTI ablation against catheter ablation with the operator blinded to contact force parameters.

Detailed description

Subjects will be followed for one year post procedure in order to check for atrial flutter recurrences. This will involve an in-person visit at 3 months post procedure, and records checks at 12 months post procedure.

Conditions

Interventions

TypeNameDescription
DEVICEContact force guided RFAContact force guided RFA during Atrial Flutter ablation procedure.

Timeline

Start date
2016-05-18
Primary completion
2020-12-01
Completion
2020-12-01
First posted
2016-07-07
Last updated
2020-05-20

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02825498. Inclusion in this directory is not an endorsement.

Randomised Prospective Trial Comparing Contact Force and Non-contact Force Guided Catheter Ablation for Cavotricuspid Is (NCT02825498) · Clinical Trials Directory