Heart patients could go home in 24 hours after valve procedure
NCT ID NCT05758909
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether people who get a new heart valve through a tube in their leg (TAVI) can safely go home just 24 hours later. Researchers will track 585 patients for complications like stroke, heart attack, or need for a pacemaker. The goal is to see if early discharge is both safe and effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could show that early discharge after TAVI is safe, leading to shorter hospital stays and faster recovery for patients.
- What could go wrong
- This is an observational study, not a randomized trial, so results may not prove cause and effect. Complications like stroke or heart issues could still occur after early discharge.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 585 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients undergoing scheduled transfemoral TAVI implantation, performed on an outpatient basis
- Ages
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18 years and older
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Patients who meet all of the following conditions will be included: * Patients ≥ 18 years undergoing transfemoral TAVI implantation scheduled, performed on an outpatient basis. * Patients with percutaneous implant. * Patients undergoing the procedure under superficial sedation or Local anesthesia. * Patients with baseline narrow QRS that does not change after implantation, or definitive pacemaker carrier. * Patients who have signed the informed consent. Exclusion Criteria: Patients who do not meet any of the following conditions: * Patients with a wide QRS (greater than or equal to 120 msec) at baseline, with the except for patients with permanent pacemakers. * Hospitalized patients undergoing urgent TAVI implantation. * Patients with access other than percutaneous transfemoral.
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hospital Clinico San Carlos
Aravaca, 28040, Spain
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Hospital Clinico Universitario de Santiago
Santiago de Compostela, 15706, Spain
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Hospital General Universitario Dr. Balmis
Alicante, 03010, Spain
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Hospital Regional Universitario de Malaga
Málaga, 29010, Spain
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Hospital Universitari Germans Trias I Pujol
Badalona, 08916, Spain
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Hospital Universitari Vall Hebron
Barcelona, 08035, Spain
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Hospital Universitari i Politècnic la Fe
Valencia, 46026, Spain
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Hospital Universitario A Coruña
A Coruña, 15006, Spain
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Hospital Universitario Central de Asturias
Oviedo, 33011, Spain
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Hospital Universitario Virgen Del Rocio
Seville, 41013, Spain
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Hospital Universitario de Bellvitge
L'Hospitalet de Llobregat, 08907, Spain
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Hospital Universitario de Navarra
Pamplona, 31008, Spain
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Hospital de Santa Creu I Sant Pau
Barcelona, 08025, Spain
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