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Completed

NCT Number: NCT04272762

A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic Atrial Fibrillation

This is a double blinded randomised placebo-controlled trial comparing the effects of catheter ablation (Cryoablation) versus a placebo procedure on atrial fibrillation burden, symptoms and quality of life

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mid and South Essex NHS Foundation Trust / The Essex Cardiothoracic Centre, Basildon, United Kingdom

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age greater than or equal to 18 years
  • Symptomatic paroxysmal or persistent atrial fibrillation despite at least one antiarrhythmic drug (AAD Type I or III, β-blocker or AAD intolerance).
  • Referred for catheter ablation

Exclusion criteria

  • Long term persistent AF (continuous episode lasting more than 1)
  • Prior left atrium catheter or surgical atrial fibrillation ablation
  • Patients with other arrhythmias requiring ablative therapy
  • Left atrium (LA) ≥5.5 cm
  • Any cardiac surgery or percutaneous coronary intervention (PCI) within three months prior to enrolment.
  • Awaiting cardiac surgery or PCI
  • Myocardial infarction within three months prior to enrolment.
  • Stroke or transient ischemic attack (TIA) within three months prior to enrolment
  • Unstable angina
  • Any significant congenital heart defect corrected or not (including atrial septal defects or PV abnormalities) but not including patent foramen ovale.
  • Any condition contraindicating chronic anticoagulation
  • Any untreated or uncontrolled hyperthyroidism or hypothyroidism
  • Severe chronic kidney disease (stage V, requiring or almost requiring dialysis, glomerular filtration rate (GFR) < 15 ml / min)
  • Patients with metallic prosthetic valves
  • Pregnant or breastfeeding women
  • Medical conditions limiting expected survival to <1 year
  • History of claustrophobia or panic attacks
  • Left ventricular ejection fraction (LVEF) less than 35%

Treatment and study plan

Cryoablation

Procedure

Pulmonary vein isolation with cryoablation

Placebo

Procedure

Placebo procedure

Primary outcomes

  1. Atrial fibrillation burden using continuous monitoring

    Time frame: 6 months

Secondary outcomes

  1. Time to symptomatic atrial tachyarrhythmia stratified by length of episode

    Time frame: 6 months

  2. Time to asymptomatic atrial tachyarrhythmia stratified by length of episode

    Time frame: 6 months

  3. Number of atrial arrhythmia ( symptomatic and asymptomatic) episodes stratified by length of episode

    Time frame: 6 months

  4. Change in AF specific quality of life score between each group (AF-PROMS)

    Time frame: Baseline and 6 months

  5. Change in health related quality of life in each group (36-Item Short Form Survey Instrument )

    Time frame: Baseline and 6 months

  6. Comparison of medical treatment ( Antiarrhythmic drug use)

    Time frame: 6 months

  7. Comparison of unscheduled use of health care services

    Time frame: 6 months

  8. Number of procedure related complications / adverse events

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

East Sussex Hospitals NHS Trust

Other

Collaborators

  • Eastbourne Cardiology Research Charity Fund
  • Medtronic

Registry information

Official study title

A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic Atrial Fibrillation (The SHAM-PVI Study)

Acronym: SHAM-PVI

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Feb 17, 2020
Registry last updated
Mar 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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