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Cardioneuroablation for Bradyarrhythmia

Study acronym: CARDIOBOOST
View on ClinicalTrials.gov ↗
Record status
This record was last updated March 5, 2024 (before its estimated February 1, 2026 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Mar 1, 2024 to Mar 4, 2024
    • Site details revised
    v3
  2. Minor Study title shortened, about 6 wordsv2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a multicenter prospective randomized blind controlled trial with a sham procedure group of the efficacy and safety of cardioneuroablation as a method of treating symptomatic bradycardia without a permanent pacemaker implantation
Trial Details
NCT Number NCT06288633
Lead Sponsor Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health
Collaborators: Meshalkin National Medical Research Center, Ministry of Health of Russian Federation, The Federal Centre of Cardiovascular Surgery, Russia, Clinical City Hospital named after I.V. Davydovsky of Moscow Department of Healthcare, City Clinical Hospital No.52 of Moscow Healthcare Department, National Medical Research Center for Therapy and Preventive Medicine, Medical Centre Hospital of the President's Affairs Administration, Republic of Kazakhstan, Tomsk National Research Medical Center of the Russian Academy of Sciences, Vishnevsky Center of Surgery, National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
Conditions
(from sponsor)
Bradycardia, Syncope, Sick Sinus Syndrome
Related terms Bradycardia, Sick Sinus Syndrome, Syncope
Enrollment 106 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov