Informations générales
  • Catégorie de maladie Maladies artérielles et veineuses y c. thrombose veineuse profonde et embolie pulmonaire (BASEC)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Lugano
    (BASEC)
  • Responsable de l'étude Idir Hamdidouche idir.hamdidouche@biotronik.com (BASEC)
  • Source(s) de données BASEC: Importé de 02.01.2026 ICTRP: N/A
  • Date de mise à jour 02.01.2026 12:50
HumRes67108 | SNCTP000006506 | BASEC2024-01834

Observational study to confirm the safety and clinical performance of the Oscar multifunctional peripheral catheter for the dilation of lesions in the femoral, popliteal, and infrapopliteal arteries

  • Catégorie de maladie Maladies artérielles et veineuses y c. thrombose veineuse profonde et embolie pulmonaire (BASEC)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Lugano
    (BASEC)
  • Responsable de l'étude Idir Hamdidouche idir.hamdidouche@biotronik.com (BASEC)
  • Source(s) de données BASEC: Importé de 02.01.2026 ICTRP: N/A
  • Date de mise à jour 02.01.2026 12:50

Résumé de l'étude

The main objective of the BIO-OSCAR First study is to confirm the safety and effectiveness of the Oscar multifunctional catheter for the dilation of narrowed arteries located in the leg. During the intervention, the Oscar Multifunctional Catheter device will be used. The patient will be treated with this and other devices according to the instructions for use, the physician's expertise, and the hospital's standards of care. Oscar is an approved and commercially available device. The following data will be collected until the patient's discharge: • The medical history and physical examination before the intervention • ABI and Rutherford measurements before the procedure, • Information related to the procedure, including angiographic images and related data • Resources used during the procedure, • Complications that may occur during the procedure until discharge.

(BASEC)

Intervention étudiée

Endovascular treatment is a minimally invasive procedure that can help open blocked arteries and allow blood to flow better. During the procedure, the study physician inserts a long, thin, flexible tube called a catheter through a small puncture in an artery in the groin. The catheter is guided through the arteries to the blocked area. Once positioned, a special balloon attached to the catheter is inflated and deflated multiple times. The balloon pushes the plaque in the artery against the walls of the artery itself, widening the vessel. If necessary, the study physician will place a tiny metal mesh tube called a stent in the area of the artery just treated with the balloon to keep it open. The stent remains permanently in the artery. Additional treatments may be performed based on the physician's expertise.

(BASEC)

Maladie en cours d'investigation

Peripheral artery disease, commonly known as peripheral vascular disease. Arteries are the blood vessels that carry oxygen-rich blood and nutrients from the heart to all areas of the body. Arteries are normally smooth and open inside, but with age, they can become blocked. A sticky substance called plaque can build up in the walls of the arteries. As plaque accumulates, the arteries narrow and harden through a process called atherosclerosis, which means hardening of the arteries. When this hardening occurs, blood flow is reduced, and the arms and legs may not receive the necessary oxygen. Doctors refer to this condition as peripheral artery disease.

(BASEC)

Critères de participation
- Rutherford classification from 2 to 6. - Reference lesion diameter between 2 and 7mm. - Vessel narrowing greater than 70% (BASEC)

Critères d'exclusion
- Previous bypass of the lesion to be treated. - Previous surgery within 30 days prior to the procedure in question. - Patient on dialysis. (BASEC)

Lieu de l’étude

Lugano

(BASEC)

non disponible

Sponsor

BIOTRONIK AG Ackerstrasse 6, 8180 Bülach, Switzerland

(BASEC)

Contact pour plus d'informations sur l'étude

Personne de contact en Suisse

Idir Hamdidouche

+41 75 429 5542

idir.hamdidouche@biotronik.com

BIOTRONIK AG Medical Affairs Ackerstrasse 6 | 8180 Bülach | Switzerland

(BASEC)

Informations scientifiques

non disponible

Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)

Commission cantonale d'éthique du Tessin

(BASEC)

Date d'approbation du comité d'éthique

28.07.2025

(BASEC)


Identifiant de l'essai ICTRP
non disponible

Titre officiel (approuvé par le comité d'éthique)
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 (BASEC)

Titre académique
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Titre public
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Maladie en cours d'investigation
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Intervention étudiée
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Type d'essai
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Plan de l'étude
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Critères d'inclusion/exclusion
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Critères d'évaluation principaux et secondaires
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Date d'enregistrement
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Inclusion du premier participant
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Sponsors secondaires
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Contacts supplémentaires
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ID secondaires
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Résultats-Données individuelles des participants
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Informations complémentaires sur l'essai
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Résultats de l'essai

Résumé des résultats

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Lien vers les résultats dans le registre primaire

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