Atrial flutter Circulatory System Atrial fibrillation and flutter
Conditions
Interventions
Study design:
A single blind 1:1:1 randomisation schedule by means of site specific sealed envelope system controlled by study administrator.
Study procedures:
Patients deemed by an electrophysiolo
Sponsors
Oxford Radcliffe Hospitals NHS Trust (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patient/subject or legal representative is willing and able to give informed consent for participation in the study 2. Male or female, aged 18 years or above 3. Diagnosed with atrial flutter
Exclusion criteria
Exclusion criteria: Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Radiofrequency time to cavotricuspid isthmus block, time from when ablation starts to when the procedure is deemed complete. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Fluoroscopy time to cavotricuspid isthmus block, the amount of x-ray screening time needed for the primary endpoint to be achieved 2. Total procedure time, includes all time, i.e., not only the primary endpoint time but any additional time of the procedure before and after | — |
Countries
United Kingdom
Outcome results
None listed