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Local Activation Time Velocity Vector-Guided Target Localization and First-site Success in Typical Atrioventricular Nodal Reentrant Tachycardia Cryoablation: A Prospective Study

Local Activation Time Velocity Vector-Guided Target Localization and First-site Success in Typical Atrioventricular Nodal Reentrant Tachycardia Cryoablation: A Prospective Study - LVV-Guided Target Localization and First-site Success in Typical AVNRT Cryoablation: A Prospective Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059700
Enrollment
30
Registered
2025-11-08
Start date
2025-11-08
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Typical atrioventricular nodal reentrant tachycardia

Interventions

Cryoablation will be performed for typical atrioventricular nodal reentrant tachycardia guided by local activation time velocity vector analysis using the CARTO3 system.

Sponsors

Gifu Prefectural General Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants who meet all of the following conditions will be enrolled: 1.Age 18 years or older. 2.Patients diagnosed with typical atrioventricular nodal reentrant tachycardia (slow-fast type) based on clinical findings and electrophysiological study. 3.Patients scheduled to undergo cryoablation with target localization guided by Local Activation Time Velocity Vector (LVV) analysis using the CARTO3 three-dimensional mapping system. 4.Patients who have received a full explanation of the study purpose and methods and have provided written informed consent. 5.Patients expected to be available for outpatient follow-up at 3 months after the procedure.

Exclusion criteria

Exclusion criteria: Participants meeting any of the following conditions will be excluded: 1.History of previous ablation for atrioventricular nodal reentrant tachycardia (AVNRT). 2.Patients whose primary arrhythmia mechanism is a manifest accessory pathway (for example, overt atrioventricular reentrant tachycardia). 3.Cases in which Kochs triangle cannot be adequately identified, making proper LVV analysis or target localization unfeasible. 4.Patients with severe atrioventricular conduction disturbance or marked bradycardia, in whom the investigator judges that study participation would compromise safety. 5.Pregnant women or those with a high likelihood of pregnancy. 6.Patients with serious comorbidities (for example, active infection or uncontrolled heart failure) that make study participation inappropriate in the judgment of the investigator. 7.Patients who are unable or unwilling to provide written informed consent, or who subsequently withdraw consent.

Design outcomes

Primary

MeasureTime frame
The proportion of cases in which non-inducibility of tachycardia is achieved by cryoablation performed only within the target area identified by Local Activation Time Velocity Vectors (LVV hot spot) (First-site success rate). In cases of failure, the reason (safety concern, insufficient effect, or technical difficulty) will be recorded.

Secondary

MeasureTime frame
1.Acute procedural success rate. 2.Number of cryoablation applications (each application defined as one 240-second freeze cycle). 3.Total cryoablation time. 4.Total procedure time. 5.Fluoroscopy time and radiation dose (dose area product: DAP). 6.Change in PQ interval (pre- and post-procedure). 7.Incidence of complications within 30 days. 8.Recurrence rate within 3 months. 9.Presence, pattern, and reversibility of atrioventricular (AV) conduction disturbances leading to cryoablation termination at the LVV-identified target region (hot-spot).

Countries

Japan

Contacts

Public ContactYoshitake Oshima

Gifu Prefectural General Medical Center Cardiology

yoshitakeoshima@gmail.com+81-582461111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026