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Biatrial global high-density electroanatomical mapping of atrial fibrillation – a prospective mechanistic registry study

Not Applicable
Conditions
Atrial fibrillation
Circulatory System
Registration Number
ISRCTN13986854
Lead Sponsor
Oxford University Hospitals NHS Foundation Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
22
Inclusion Criteria

1. Participant is willing and able to give informed consent for participation in the trial
2. Male or female, aged 18 years or above
3. Diagnosed with paroxysmal or persistent atrial fibrillation and planned for a catheter ablation procedure
4. In the Investigator’s opinion is able and willing to comply with all trial requirements

Exclusion Criteria

1. Physical or anatomical barriers to the use of two simultaneous mapping catheters
2. Previous cardiac surgery
3. Previous ablation (catheter or surgical)
4. Female participant who is pregnant, lactating or planning pregnancy during the course of the trial
5. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant’s ability to participate in the trial
6. Participants who have participated in another research trial involving an investigational medicinal product in the past 12 weeks. (Involvement in any other research trial is not a contraindication per se)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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