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CMR based myocardial tissue characterization in correlation with functional and flow-dynamic processes in patients with severe aortic stenosis prior to and after TAVI

Not Applicable
Conditions
I35.0
Aortic (valve) stenosis
Registration Number
DRKS00009370
Lead Sponsor
niklinik KölnInstitut für Diagnostische und Interventionelle Radiologie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
90
Inclusion Criteria

Patients with severe aortic stenosis who will undergo a TAVI procedure.
Control group: Healthy volunteers without any known heart disease.

Exclusion Criteria

MR contraindications (pacemakers, insulin pumps, cochlea implants, etc.); severe renal insufficiency (GFR < 30 ml/min); hemodynamic significant heart insufficiency that would lead to relevant additional stress for the patient during the examination.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
After acquisition of CMR data before and 6 months after TAVI, all data (T1, strain, flow parameters, volumetry, late enhancement) will be quantified using various software algorithms. All data of both examinations will be compared to the group of healthy volunteers.
Secondary Outcome Measures
NameTimeMethod
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