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Search / Trial NCT03938090

Optimised MultiSite Pacing Vector Study

Launched by BARTS & THE LONDON NHS TRUST · May 2, 2019

Trial Information

Current as of May 28, 2025

Withdrawn

Keywords

Cardiac Resynchronization Therapy Multi Site Pacing

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Symptomatic Heart Failure (NYHA class I-IV) with QRS duration of 150ms or more with left bundle branch block and LVEF of 35% or less despite optimal medical therapy.
  • Patients above 18 years of age
  • Able to provide informed consent and willing to comply with study requirements
  • Intrinsic QRS duration ≥ 150 ms
  • Sinus (or atrial paced) rhythm with intact AV conduction (PR interval ≤250 ms)
  • Exclusion Criteria:
  • Resting heart rate \> 100 bpm
  • High degree AV Block (2nd or 3rd degree AV block)
  • Documented persistent atrial arrhythmia at the moment of enrolment or patients not likely to remain in sinus (or atrial paced) rhythm for the duration of the study
  • Patients scheduled for AV node ablation to treat atrial arrhythmias
  • Recent (\< 3 months) myocardial infarction, catheter ablation, electrolyte imbalance, or any condition within the last 90 days that would contraindicate CRT programming changes in the opinion of the investigator
  • Women who are pregnant or plan to become pregnant during the study course
  • Known left ventricular thrombus

About Barts & The London Nhs Trust

Barts and The London NHS Trust is a leading healthcare organization in the United Kingdom, renowned for its commitment to delivering high-quality clinical care, research, and education. As a prominent sponsor of clinical trials, the Trust is dedicated to advancing medical knowledge and improving patient outcomes through innovative research initiatives. With a focus on patient safety and ethical standards, Barts and The London NHS Trust collaborates with multidisciplinary teams to explore cutting-edge therapies and interventions across various medical fields, ensuring that trial participants receive the highest level of care and support throughout their involvement.

Locations

London, , United Kingdom

Patients applied

0 patients applied

Trial Officials

Anthony WC Chow, MBBS BSc MD

Principal Investigator

Study Chief Investigator

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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