Last reviewed · How we verify
NCT05196126: SANOK
Permanent Pacemaker Implantation or Cardioneuroablation in Sinus Node Dysfunction
NA trial testing Permament pacemaker implantation in Sinus Node Dysfunction in 60 participants. Status unknown.
31 May 2024
Quick facts
| Lead sponsor | Stec, Sebastian, MD, PhD, FESC |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 1 June 2022 |
| Primary completion | 31 May 2024 |
| Estimated completion | 30 June 2024 |
| Sites | 4 locations across Poland |
Drugs / interventions tested
- Permament pacemaker implantation
- Cardioneuroablation
Conditions studied
- Sinus Node Dysfunction — all drugs for Sinus Node Dysfunction →
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):
-
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
Verify or expand the search:
- PubMed search for NCT05196126
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Sinus Node Dysfunction
Currently open trials in the same condition.
- NCT07209852 — Safety, Performance, and Clinical Benefit of Pacing the Left Bundle Branch Area - Post-Market Clinical Follow-up · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05196126 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Stec, Sebastian, MD, PhD, FESC
- Last refreshed: 7 March 2023
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.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing