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Clinical Trials/NCT03085693
NCT03085693
Active, not recruiting
Not Applicable

Impact of Left Atrial Appendage Closure With a Closure Device on Quality of Life, Physical Capacity and Expression of Atrial Natriuretic Peptide and Brain Natriuretic

University of Leipzig1 site in 1 country40 target enrollmentAugust 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation
Sponsor
University of Leipzig
Enrollment
40
Locations
1
Primary Endpoint
exercise capacity measured by maximal oxygen consumption
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

Closure of the left atrial appendage in patients with atrial fibrillation and risk for stroke is a increasing technology leading to exclusion of the left atrial appendage volume from the blood circulation and therefore protects from cardioembolic strokes- It is unclear if the volume reduction of the left atrium leads to a change in exercise capacity or Quality of life.

Detailed Description

The monocentric trial deals with the endocrinological changes as a result of closure of the left atrial appendage with a internal closure device. Specially, the changes in atrial natriuretic peptide, brain natriuretic peptide and their impact on exercise capacity is on focus of the trial. The trial is planned as a all comers trial.

Registry
clinicaltrials.gov
Start Date
August 2016
End Date
November 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Leipzig
Responsible Party
Principal Investigator
Principal Investigator

Sven Möbius-Winkler

PD Dr. med.

University of Jena

Eligibility Criteria

Inclusion Criteria

  • Patient with a indication for LAA closure device Implantation

Exclusion Criteria

  • Inability to perform exercise testing

Outcomes

Primary Outcomes

exercise capacity measured by maximal oxygen consumption

Time Frame: Baselina, 45 days, 6 months

Change from baseline spiroergometry to 45 days to 6 months

Study Sites (1)

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