RecruitingNot ApplicableNCT07456280

Pilot Study to Evaluate a Noninvasive Electrocardiographic Monitoring Strategy Associated With Early Discharge in Patients With Conduction Disorders Following TAVI Implantation (IMPROVE Study)


Sponsor

Hospital Universitari Vall d'Hebron Research Institute

Enrollment

100 participants

Start Date

Jul 20, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Study to evaluate the efficacy and safety of a non-invasive electrocardiographic monitoring strategy associated with early discharge in patients with conduction disorder after transfemoral TAVI implantation, and its potential benefits compared to standard care.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called PhysioMem PM 100 4G ambulatory monitoring system and a behavioral approach called Standard care for people with cardiovascular diseases and severe aortic valve stenosis. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALStandard care

Patients discharged according to standard care

DEVICEPhysioMem PM 100 4G ambulatory monitoring system

Patients discharged with PhysioMem PM 100 4G ambulatory monitoring system


Locations(1)

Hospital Unniversitari Vall d'Hebron

Barcelona, Spain

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07456280


Related Trials