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Search / Trial NCT01057485

Node and Atrial Fibrillation Ablation for Persistent Atrial Fibrillation

Launched by EASTBOURNE GENERAL HOSPITAL · Jan 26, 2010

Trial Information

Current as of June 07, 2025

Unknown status

Keywords

Atrial Fibrillation Ablation

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients with symptomatic drug refractory atrial fibrillation.
  • Patients who have had pacemaker implantation and AV node ablation with ongoing symptoms.
  • Patients will already be refractory to at least 2 rate or rhythm control drugs.
  • Patients must be over 18 years old.
  • Patients give informed consent form prior to participating in this study.
  • Exclusion Criteria:
  • Patient is suffering with unstable angina in last 1 week.
  • Patient has had a myocardial infarction within last 2 months.
  • Patient is expecting or has had major cardiac surgery within last 2 months.
  • Patient is participating in a conflicting study.
  • Patient is unable to perform exercise testing.
  • Patient is mentally incapacitated and cannot consent or comply with follow-up.
  • Patient has NYHA class III/ IV heart failure.
  • Patient has LVEF \<35% not secondary to tachycardia.
  • Pregnancy.
  • Patient suffers with other cardiac rhythm disorders.
  • Recent coronary artery intervention or other factors suggesting clinical instability (ECG, clinical or laboratory findings).

About Eastbourne General Hospital

Eastbourne General Hospital is a leading healthcare facility dedicated to advancing medical research and improving patient outcomes through innovative clinical trials. As a trusted sponsor, the hospital collaborates with multidisciplinary teams to design and implement studies that address pressing health challenges. With a commitment to ethical standards and patient safety, Eastbourne General Hospital aims to contribute valuable insights to the medical community and enhance treatment options for diverse populations. Their state-of-the-art resources and experienced staff ensure robust trial management and data integrity throughout the research process.

Locations

Eastbourne, East Sussex, United Kingdom

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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