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Study identifier: NCT04029844 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Colibri Transcatheter Aortic Heart Valve System Study

Condition: Severe Aortic Stenosis  ·  Sponsor: Colibri Heart Valve LLC

PhaseNA
Planned participants30
Who can joinAll sexes, 75 Years to no upper limit
Healthy volunteersNo

About this study

The Colibri Heart Valve clinical investigation ("COL-01") is a prospective, multicenter, exploratory single arm and controlled clinical investigation compared to recent historical results. This study will be conducted in about 7 European sites. The study will evaluate the safety and performance of the Colibri Transcatheter Aortic Heart Valve System for the treatment of symptomatic severe aortic stenosis via transfemoral access in high surgical risk patients. 30 subjects suffering from symptomatic severe aortic tricuspid valve stenosis and who are at high surgical risk (logistic EuroSCORE I \> 20% or other risk factors not included in this score such as frailty, porcelain aorta, sequelae of chest radiation or logistic EuroSCORE I \< 20% but considered at high risk by local Heart Team evaluation) will be enrolled in this clinical investigation. The primary objective of this clinical investigation is to evaluate the all-cause mortality at 30 days post implantation. The secondary objectives are to evaluate the safety and performance of the investigational device at 30 days, 6 and 12 months, and 2, 3, 4, 5 years post implantation.

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

Talk to the study team

R David Fish, MD  ·  1 (303) 460 8667  ·  colibriTAVI@colibrihv.com

Always discuss trial participation with your own doctor first.

Locations (5)

Institut Coeur Poumon, CHRULille, FranceRecruiting
Hôpital Privé Jacques CartierMassy, FranceRecruiting
Clinique PasteurToulouse, FranceRecruiting
Brighton & Sussex University Hospital, Roayl Sussex County HospitalBrighton, East Sussex, United KingdomRecruiting
Barts Heart Centre / St Bartholomew's HospitalLondon, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT04029844