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Telemedicine monitoring of patients with severe aortic stenosis and planned transcatheter aortic valve implantation (TAVI) under normal conditions and when treatment capacity is limited due to crisis.

Not Applicable
Recruiting
Conditions
I35.0
Aortic (valve) stenosis
Registration Number
DRKS00027842
Lead Sponsor
Charité Campus Charité Mitte
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

Patient with decision for TAVI in case of severe aortic stenosis in the heart team, age of majority, written consent of the patient.

Exclusion Criteria

Inability or unwillingness to take daily vital signs (e.g., dementia, blindness, deafness, wheelchair use, insufficient German language skills, limited informal self-determination), Participation in therapy studies (observational studies and registries are possible).

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Days lost due to unplanned cardiovascular hospitalisations and all-cause mortality up to 180 days after heart team decision
Secondary Outcome Measures
NameTimeMethod
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