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NCT05196126: SANOK

Permanent Pacemaker Implantation or Cardioneuroablation in Sinus Node Dysfunction

Status unknown NA Last updated 7 March 2023
What this trial tests

NA trial testing Permament pacemaker implantation in Sinus Node Dysfunction in 60 participants. Status unknown.

Timeline
1 June 2022
Primary endpoint
31 May 2024
30 June 2024

Quick facts

Lead sponsorStec, Sebastian, MD, PhD, FESC
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment60
Start date1 June 2022
Primary completion31 May 2024
Estimated completion30 June 2024
Sites4 locations across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Stec, Sebastian, MD, PhD, FESC

Who can join

Adults 18 to 75, any sex, with Sinus Node Dysfunction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a noncommercial, physician-initiated, monitored, multicenter, prospective randomized clinical trial, a proof-of-concept study, investigating a treatment strategy only. The study will use medical products applied for invasive and nonivasive procedures performed at the participating centers.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Rationale and design of SAN.OK randomized clinical trial and registry: Comparison of the effects of evidence-based pacemaker therapy and cardioneuroablation in sinus node dysfunction.
    Stec S, Jankowska-Polańska B, Jagielski D, Wileczek A, et al · · 2022 · cited 5× · PMID 36385604 · DOI 10.5603/cj.a2022.0103

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Other recruiting trials for Sinus Node Dysfunction

Currently open trials in the same condition.

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Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05196126.

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