Aortic Valve Stenosis Clinical Trials

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Measuring Outcomes in Aortic STenosis Patients Undergoing AVR - Evaluation of Prognosis Regarding Short- and Long-term Results (MASTER)

Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY

The investigators will prospectively enroll 300 patients undergoing TAVI at Sahlgrenska University Hospital, which is the second largest TAVI hospital in Sweden. Eligible patients should have a clinical indication for aortic valve replacement with TAVI and have preprocedural clinical investigations with echocardiography (UCG) and CCT and provide written informed consent. UCG, electrocardiogram (ECG) and blood samples will be taken in addition to clinical status, NYHA-class and collection of outcome events the day before the procedure, 1±2 hours, 24 ±6hours and daily after the procedure until discharged from Sahlgrenska. Further follow-up will be scheduled day 14, 30, 180, 365 and yearly. Cardiac MRI will be performed before, at 14 days and at 180 days after TAVI. Brain MRI will be performed before and 24± hours after TAVI. Cardiac CT will be performed at 180 days after TAVI.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Patient with clinical indication for aortic valve replacement and scheduled for TAVI

• Patient willing and able to provide signed informed consent

Locations
Other Locations
Sweden
Departement of Cardiology
RECRUITING
Gothenburg
Departement of Cardiology,
RECRUITING
Gothenburg
Contact Information
Primary
Oskar Angerås, MD, PhD
oskar.angeras@vgregion.se
+46 313421000
Backup
Björn Redfors, MD, PhD, Professor
bjoern.redfors@wlab.gu.se
031342100
Time Frame
Start Date: 2025-03-04
Estimated Completion Date: 2031-06
Participants
Target number of participants: 300
Treatments
TAVI patients
300 patients undergoing TAVI at Sahlgrenska University Hospital
Related Therapeutic Areas
Sponsors
Leads: Vastra Gotaland Region

This content was sourced from clinicaltrials.gov