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Improving Patient Reported Outcome Measures in Catheter Ablation

RecruitingNAAges 18 Years - anyAllBarts & The London NHS Trust
NCT04499326 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study will assess whether more frequent measurement of patient reported outcome measures (PROMs) - specifically health related quality of life (HRQL) - can improve the evaluation of the clinical effectiveness and cost-effectiveness of catheter ablation of ventricular tachycardia (VT) in patients with an Implantable Cardioverter Defibrillator (ICD). It is designed to have feasibility outcomes which contribute to answering the above.

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📋 Eligibility rules (as published)
Inclusion Criteria: Adults (\>18 years) With an Implantable Cardioverter Defibrillator (ICD) implanted \>3 months from time of recruitment and a previous episode of documented VT requiring therapy from the ICD. And impaired LV/RV function Willing and able to give written informed consent Exclusion Criteria: Patients who are planning to move away from study site within 12 months of enrolment who wished to use postal method to complete their HRQL Patients who are unable to give informed consent
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What it tests

  • Validated quality of life questionnaire (EQ-5D & C-CAP)
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Where

1 site
St Bartholomew's Hospital
London, United Kingdom
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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