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A Cohort Study to Evaluate the Safety and Efficacy of the Temporary Permanent Pacemaker in Patients with Conduction Block after TAVR

A Cohort Study to Evaluate the Safety and Efficacy of the Temporary Permanent Pacemaker in Patients with Conduction Block after TAVR

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057931
Enrollment
Unknown
Registered
2022-03-22
Start date
2022-03-09
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

Aortic valve disease

Interventions

None listed

Sponsors

Beijing Anzhen Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Secondary type I and above atrioventricular block occurred during rapid pacing in the central chamber of TAVR (120 beats/min); 2. Third-degree atrioventricular block occurred from intraoperative to postoperative 1 month for TAVR; 3. Second degree type II atrioventricular block occurred from intraoperative to 1 month after TAVR; 4. Second degree type I atrioventricular block occurred from intraoperative to postoperative 1 month for TAVR; 5. One degree of atrioventricular block with obvious symptoms (PR interval > 300 ms) occurred during the operation to 1 month after TAVR; 6. Alternate bundle branch block occurred in TAVR from intraoperative to 1 month after operation; 7. After TAVR, symptoms related to double branch block with fainting or black outside occurred during the operation to 1 month after the operation; 8. During the operation to 1 month after the operation of TAVR, PR or QRS was prolonged >= 20 ms from baseline, accompanied by bundle branch block (QRS > 150 ms) and first-degree atrioventricular block (PR > 240 ms).

Exclusion criteria

Exclusion criteria: 1. Permanent pacemaker was implanted before TAVR; 2. TAVR has indications of permanent pacemaker implantation before operation; 3. Conduction block caused by other diseases (such as neuromuscular diseases); 4. Patients had poor compliance and could not complete the study as required.

Design outcomes

Primary

MeasureTime frame
Rate of removing temporary pacemaker;

Secondary

MeasureTime frame
Rate of Permanent Pacemaker Implantation;

Countries

China

Contacts

Public ContactGuangyuan Song

Beijing Anzhen Hospital, Capital Medical University

songgy_fuwai@vip.163.com+86 13801120805

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026