Frontlight ResearchEarly access
Active, not recruitingNo phase
Evaluation of the Viability and Safety of Early Discharge Protocol After TAVI Implantation
Key facts
- Who runs it
- Fundación EPIC
- Where
- Spain13 sites in 1 countryChoose a country to see its sites
- Trial code
- Status
- Active, not recruiting
- People taking part
- 585 people, planned
- Started
- 4 Apr 2023
- Expected to end
- 1 Dec 2026
- Type of study
- Observational
- Treatments tested
- TF TAVI
- Record updated
- 19 December 2025
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
The registry criteria, word for word
Show all 10 criteriaShow less
Who can take part
- 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
Who cannot take part
- 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
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
Evaluation of the safety and efficacy of early discharge (24 hours) after transfemoral transcatheter aortic prosthesis implantation (TAVI).
The group in the trial
- Patients receiving transfemoral (TF) TAVI
TF TAVI
Treatment: TF TAVI
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Record updated
- 19 December 2025