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Study identifier: NCT06758921 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Prospective, Multicenter, Single-Arm Observational Study to Confirm the Safety and Clinical Performance of the Oscar Peripheral Multifunctional Catheter for the Dilatation of Lesions in the Femoral, Popliteal and Infrapopliteal Arteries (BIO-OSCAR First)

Condition: Peripheral Arterial Disease · Peripheral Arterial Disease(PAD)  ·  Sponsor: Biotronik AG

PhaseN/A
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the standard of care practices, procedural outcomes, and in-hospital complications for endovascular peripheral interventions of femoral, popliteal and infrapopliteal lesions.

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

Talk to the study team

Helene Kuissu, PharmD  ·  +41 44 864 54 80  ·  helene.kuissu@biotronik.com

Always discuss trial participation with your own doctor first.

Locations (16)

LKH Univ. -Klinikum Graz, Ambulanz für AngiologieGraz, AustriaRecruiting
Onze Lieve VrouwziekenhuisAalst, BelgiumNot Yet Recruiting
AZ Saint BlasiusDendermonde, BelgiumRecruiting
ZOL Ziekenhuis Oost LimburgGenk, BelgiumNot Yet Recruiting
University Hospital GhentGhent, BelgiumNot Yet Recruiting
vzw AZ GroeningeKortrijk, BelgiumNot Yet Recruiting
Hopital Saint JosephParis, FranceNot Yet Recruiting
Karolinen-Hospital ArnsbergArnsberg, GermanyNot Yet Recruiting
Sankt Gertrauden-KrankenhausBerlin, GermanyNot Yet Recruiting
Universitätsklinikum TübingenTübingen, GermanyNot Yet Recruiting
Semmelweis UniversityBudapest, HungaryNot Yet Recruiting
Policlinico Abano TermeAbano Terme, ItalyNot Yet Recruiting

+ 4 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06758921