Conduct: Edwards SAPIEN 3 PPI Registry

Sponsor
Institut für Pharmakologie und Präventive Medizin (Other)
Overall Status
Completed
CT.gov ID
NCT03497611
Collaborator
Edwards Lifesciences (Industry)
1,000
4
10.1
250
24.8

Study Details

Study Description

Brief Summary

There are patient related risk factors for PPI that can be identified and assessed in retrospective pooling of 1000+ TAVI patient datasets.

Retrospective pooling of 6 datasets already available at participating centres (4 sites in Germany, 1 in Zwolle / The Netherlands, 1 in Linköping / Sweden).

Additional assessment of calcifications using a CT data core lab. Statistical analysis of the obtained dataset with respect to the objectives of the registry.

Condition or Disease Intervention/Treatment Phase
  • Procedure: transcatheter valve implantation

Detailed Description

Permanent pacemaker implantation is a widely recognized clinical event associated with TAVI becoming evident within a few days after the procedure.

While a number of registries have documented the rates of PPI with different valves, much less evidence has been provided for 1) patient based characteristics (e.g. RBBB etc.) affecting the likelihood of PPI and for 2) procedural variables (e.g. implantation depth, valve size etc.) that should be considered to perform an as safe and minimal invasive procedure as possible.

Prior research To date there are 7 published reports on pacemaker rates and predictors associated with the use of the Edwards SAPIEN 3 THV (see Table). These studies suggest that the need for pacemaker implantation in single centers ranges between 14.4 and 20.4% derived from patient numbers between 131 and 335. These analyses resulted in the identification of pre-existing conduction disturbance / aortic valve calcification as patient related and implantation depth /oversizing as procedure related variables associated with Edwards SAPIEN 3 THV TAVI. Furthermore a scoring algorithm for patient related factors has been proposed from a dataset of 240 patients to predict the likelihood of PPI after THV .

Limitations of prior research Current evidence though is limited by patient numbers versus event rates (with a max. of 62 PPI considered in any of the available datasets) resulting in a limited power in multivariable analyses, the single center design of these ventures, the lack of a consistent definition of variables potentially associated and the unexplained differences in the number and type of variables identified.

Aims For this reason the investigators consider it necessary to 1) to retrospectively pool data from all of these 7 datasets to arrive at a more comprehensive picture of patient related variables (retrospective part I), to 2) assess procedural variables in a prospective multicenter registry (prospective part II) and 3) to potentially validate the identified variables in a future prospective cohort.

Study Design

Study Type:
Observational
Actual Enrollment :
1000 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Edwards SAPIEN 3 PPI Registry - A Retrospective Survey and Prospective Identification of Procedure Related Variables Associated With Permanent Pacemaker Implantation in Patients Receiving an Edwards SAPIEN 3 Valve
Actual Study Start Date :
Apr 30, 2018
Actual Primary Completion Date :
Nov 3, 2018
Actual Study Completion Date :
Mar 3, 2019

Arms and Interventions

Arm Intervention/Treatment
Patients with aortic stenosis

Patients receiving Edwards SAPIEN 3 Transcatheter aortic valve implantation

Procedure: transcatheter valve implantation
aortic transcatheter valve implantation using Edwards SAPIEN 3 valve

Outcome Measures

Primary Outcome Measures

  1. occurence of PPI after TAVI [30 days]

    need for permanent pacemaker implantation after TAVI

Secondary Outcome Measures

  1. Timing of PPI [30 days]

    Time interval after TAVI until PPI in days

  2. Indications for PPI [30 days]

    possible reasons to implant a PP: 1° AV block complete RBBB complete LBBB QRS duration prolonged LVOT calcium volume below the left and right cusp etc

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients that already underwent Edwards SAPIEN 3 implantation because of aortic stenosis
Exclusion Criteria:
  • Patients with prior pacemaker or intended valve in valve implantation

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Clinic Tübingen, Department of Internal Medicine III Tübingen Baden-Württemberg Germany 72076
2 University Clinic Ulm, Department of Internal Medicine II Ulm Baden-Württemberg Germany 89073
3 Herzzentrum, Universität Köln Cologne Nordrhein-Westfalen Germany 50937
4 Universitätsklinikum Münster, Klinik und Poliklinik für Erwachsene mit angeborenen und erworbenen Herzfehlern Münster Nordrhein-Westfalen Germany 48149

Sponsors and Collaborators

  • Institut für Pharmakologie und Präventive Medizin
  • Edwards Lifesciences

Investigators

  • Principal Investigator: Tobias Geisler, Prof., University Clinic Tübingen, Tübingen, Germany - Department of Internal Medicine III

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institut für Pharmakologie und Präventive Medizin
ClinicalTrials.gov Identifier:
NCT03497611
Other Study ID Numbers:
  • Conduct
First Posted:
Apr 13, 2018
Last Update Posted:
Sep 4, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Institut für Pharmakologie und Präventive Medizin
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 4, 2020