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NCT07348991
Predicting Severe Cardiac Arrhythmias in the Perioperative Period Using AI-ECG
trial testing digital single-channel ECG recording in Atrial Fibrillation in 300 participants. Not yet recruiting.
30 June 2027
Quick facts
| Lead sponsor | I.M. Sechenov First Moscow State Medical University |
|---|---|
| Status | Not yet recruiting |
| Study type | OBSERVATIONAL |
| Enrollment | 300 |
| Start date | 31 December 2026 |
| Primary completion | 30 June 2027 |
| Estimated completion | 30 May 2028 |
Drugs / interventions tested
- digital single-channel ECG recording
Conditions studied
- Atrial Fibrillation — all drugs for Atrial Fibrillation →
- Atrioventricular Block, Second and Third Degree — all drugs for Atrioventricular Block, Second and Third Degree →
- Sinus Node Dysfunction — all drugs for Sinus Node Dysfunction →
- Ventricular Tachycardia (VT) — all drugs for Ventricular Tachycardia (VT) →
Sponsor
I.M. Sechenov First Moscow State Medical University
Who can join
18 and older, any sex, with Atrial Fibrillation or Atrioventricular Block, Second and Third Degree. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
During the preoperative examination, in addition to the standard examination recommended before high-risk cardiac surgeries, a digital single-lead ECG is recorded using portable CardioQUARK devices. This ECG is analyzed for time, amplitude, and frequency parameters-more than 200 parameters per cardiac cycle. Additionally, the available parameters of a standard 12-lead ECG recording are determined. All parameters of both single-lead and 12-lead ECGs will be included in a multivariate regression analysis to determine the optimal method for predicting atrial fibrillation, life-threatening cardiac arrhythmias, and conduction abnormalities in the perioperative period after high-risk cardiac procedures. The study will include patients undergoing high-risk cardiac surgeries, such as those on the heart, aorta, esophagus, pancreas, liver, and lungs, as well as high-risk oncological surgeries. A partial analysis will also be performed depending on the type of intervention. Rhythm and conduction disturbances will be recorded during surgery, as well as in the postoperative period, using ECG monitors, 24-hour ECG monitoring, and repeated recordings of a standard ECG when complaints or signs of unstable hemodynamics arise
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07348991
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other I.M. Sechenov First Moscow State Medical University trials
Trials by the same sponsor.
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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 NCT07348991 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by I.M. Sechenov First Moscow State Medical University
- Last refreshed: 10 February 2026
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/NCT07348991.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing