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EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensity Focused Ultrasound

NCT01769287 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2017-09-19

No results posted yet for this study

Summary

The purpose of this study is to check if at 1 year after surgical ablation the electrical impulses that cause atrial fibrillation (AF) are still blocked from being able to get into the heart.

Hypothesis Conduction block and ganglionic destruction are required for freedom from AF.

Conditions

Sponsors & Collaborators

  • Abbott Medical Devices

    collaborator INDUSTRY

  • University Hospital Plymouth NHS Trust

    lead OTHER

Principal Investigators

  • Malcolm Dalrymple-Hay, MB BS, PhD · University Hospital Plymouth NHS Trust

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • United Kingdom

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01769287 on ClinicalTrials.gov