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Swedish Study on STroke After TAVR

NCT ID: NCT04086836

Last Updated: 2020-04-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

4600 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-07-01

Study Completion Date

2020-02-01

Brief Summary

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This study aims at studying the frequency of late stroke after transcatheter aortic valve replacement/implantation

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Detailed Description

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Since the start of transcatheter aortic valve implnatations/replacements (TAVR/TAVI) implantations in Sweden in 2008 all procedures have been added to a national database, which now contains 5000+ procedures. At the same time, all admissions to the hospital is also recorded with diagnosis in a separate database. We intend to make a nation-wide complete follow up of all TAVR/TAVI patients in swede that has received the diagnosis of stroke after the implantation. In addition data will also be collected from the national stroke database for detailed information of the cases

Conditions

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Aortic Valve Disease Stroke

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patient suffering a late stroke after TAVR

All patients suffering a stroke after TAVR will be studied

TAVR

Intervention Type DEVICE

Patient recieving a TAVR

Interventions

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TAVR

Patient recieving a TAVR

Intervention Type DEVICE

Eligibility Criteria

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Exclusion Criteria

Periprocedural stroke
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Region Skane

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Skane University Hospital

Lund, , Sweden

Site Status

Countries

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Sweden

Other Identifiers

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SWESTAT

Identifier Type: -

Identifier Source: org_study_id

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