Sinus Node Dysfunction

2

Review clinical trials related to Sinus Node Dysfunction. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Safety, Performance, and Clinical Benefit of Pacing the Left Bundle Branch Area - Post-Market Clinical Follow-up

The goal of this observational post-market clinical Follow-up study is to learn about the long-term safety, performance, and clinical benefits of pacing the left bundle branch area (LBBAP) using the INGEVITY+ pacemaker lead in patients with bradycardia who need a pacemaker.

Participants needed: 140
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Boston Scientific CorporationUpdated: Jun 4, 2026Locations: 13Duration: 3 Years
Eligibility criteria

Subjects intended to undergo initial (de novo) pacing system implant using the I... [+11]

Subjects meeting guideline indications for cardiac resynchronization therapy (CR... [+10]

Status: Not yet recruiting

Predicting Severe Cardiac Arrhythmias in the Perioperative Period Using AI-ECG

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

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: I.M. Sechenov First Moscow State Medical UniversityUpdated: Feb 10, 2026
Eligibility criteria

Patients over 18 years of age; [+2]

Cancellation of the surgery for any reason; [+2]