Actively Recruiting

Age: 18Years +
All Genders
ID01390675

Anesthesia for Catheter Aortic Valve ImplantATIOn Registry

Led by Deutsches Herzzentrum Muenchen · Updated on 2024-08-07

10000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying patients undergoing transcatheter aortic valve implantation (TAVI), an emerging procedure used in high-risk cardiac surgery and cardiology patients who are often considered inoperable by conventional means. This observational study aims to understand the specific anesthesiologic challenges faced by cardiac anesthesiologists during these procedures. The study is sponsored by Deutsches Herzzentrum Muenchen and focuses on improving perioperative care in this high-risk group. This study involves monitoring patients who receive TAVI, without any experimental treatments or interventions. The study observes the anesthesia process and perioperative care during the procedure. There are no comparison groups or drug treatments involved. Participants will be observed during the perioperative period, specifically for one day around the time of the procedure. Researchers will collect data on anesthesiology care and related cardiac events during the operation. Additionally, participants may be followed for up to 10 years to assess longer-term outcomes. The study does not involve any additional treatments and focuses on collecting observational data to better understand anesthesia management in TAVI.

CONDITIONS

Brief Title

Anesthesia for Catheter Aortic Valve ImplantATIOn Registry

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing transcatheter aortic valve implantation (TAVI)
Not Eligible

You will not qualify if you...

  • Refusal by patient

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - 1 day

Participants who undergo routine care for transcatheter aortic valve implantation are observed during perioperative care.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 10 years

Participants are followed for up to 10 years to observe long-term outcomes after the procedure.

Trial Site Locations

Total: 1 location

1

Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München

Munich, Bavaria, Germany, D-80636

Actively Recruiting

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Research Team

P

Patrick N Mayr, M.D.

M

Michael Joner, M.D.,Prof

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Dexmedetomidine versus propofol-opioid for sedation in transcatheter aortic valve implantation patients: a retrospective analysis of periprocedural gas exchange and hemodynamic support.

N Patrick Mayr, Gunther Wiesner, Pieter van der Starre...

https://pubmed.ncbi.nlm.nih.gov/29464420