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Study identifier: NCT07532733 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Respiratory and Haemodynamic Effects of Conscious Sedation With Dexmedetomidine for a TAVI Procedure

Condition: TAVI(Transcatheter Aortic Valve Implantation)  ·  Sponsor: Erasme University Hospital

PhaseNA
Planned participants80
Who can joinAll sexes, 60 Years to no upper limit
Healthy volunteersNo

About this study

Transcatheter aortic valve implantation (TAVI) is now the standard procedure for elderly patients with severe aortic stenosis. This patient group is characterised by increased frailty, multiple comorbidities and limited physiological reserve, exposing them to an increased risk of intraoperative complications. The majority of TAVI procedures are now performed under conscious sedation, in order to limit the risks associated with general anaesthesia and to promote a faster recovery. However, this strategy carries a risk of intraoperative respiratory events, notably bradypnoea, oxygen desaturation and airway obstruction, particularly in elderly patients with comorbidities. The anaesthetic strategy, and in particular the type of sedation used, is likely to influence intraoperative respiratory and haemodynamic tolerance. Traditionally used agents, such as propofol combined with opioids, can induce dose-dependent respiratory depression. Conversely, dexmedetomidine, an α2-adrenergic receptor agonist, has a distinct pharmacological profile, characterised by sedation with a theoretically limited respiratory impact. However, comparative data regarding the impact of different sedation strategies on intraoperative respiratory tolerance during TAVI remain limited, justifying the conduct of this study. Dexmedetomidine is a selective α2-adrenergic receptor agonist, used in anaesthesia and intensive care for its sedative and anxiolytic properties. It induces what is known as 'cooperative'…

This description comes directly from the study's public registry record.

Talk to the study team

Celine Boudart, MD PhD  ·  +3225553919  ·  celine.boudart@hubruxelles.be

Always discuss trial participation with your own doctor first.

Locations (1)

HUB ErasmeBrussels, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT07532733