Regression in Left Ventricular Hypertrophy and Fibrosis in Aortic Stenosis
NCT07539259
Aortic Stenosis, Aortic Valve Disease
View Trial DetailsNCT Number: NCT06870734
Transcarotid transcatheter aortic valve replacement (Transcarotid TAVR) has been increasingly used as an alternative to the transfemoral approach. The general anesthesia, locoragional anesthesia or local anesthesia are three anesthesia techniques that can be used for transcarotid TAVR. We aim to compare the locoregional approach to gerneral anesthesia.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 7 days
Composite endpoint combining mortality and stroke in the first post-operative week
Time frame: 7 days
Death occuring during the first week after intervention
Time frame: 7 days
Stroke occuring during the first week after the intervention
Time frame: 30 days
Death occuring during the first month after intervention
Time frame: 1 year
Death occuring during the first year after intervention
Time frame: 1 day
Use of vasopressive drugs during the intervention
Time frame: 7 to 30 days
Pacemaker implantation during the index hospitalisation
Trial opening soon.
Get NotifiedUniversity Hospital, Caen
Other
General Anesthesia Versus Loco-Regional Anesthesia for Transcarotid Trancatheter Aortic Valve Replacement - a Retrospective Cohort Study
Acronym: GALATTAVI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07539259
Aortic Stenosis, Aortic Valve Disease
View Trial DetailsNCT07806409
Aortic Stenosis, Aortic Stenosis Senile
View Trial DetailsNCT07756398
Aortic Stenosis, Aortic Valve Disease
Dallas, Texas, United States
View Trial DetailsNCT07739316
Aortic Stenosis, Aortic Valve Disease
Québec, Quebec, Canada
View Trial Details