Informazioni generali
  • Categoria della malattia Malattie arteriose e venose incluse la trombosi venosa profonda e l'embolia polmonare (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Lugano
    (BASEC)
  • Responsabile dello studio Idir Hamdidouche idir.hamdidouche@biotronik.com (BASEC)
  • Fonte dati BASEC: Importato da 02.01.2026 ICTRP: N/A
  • Ultimo aggiornamento 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

  • Categoria della malattia Malattie arteriose e venose incluse la trombosi venosa profonda e l'embolia polmonare (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Lugano
    (BASEC)
  • Responsabile dello studio Idir Hamdidouche idir.hamdidouche@biotronik.com (BASEC)
  • Fonte dati BASEC: Importato da 02.01.2026 ICTRP: N/A
  • Ultimo aggiornamento 02.01.2026 12:50

Descrizione riassuntiva dello studio

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)

Intervento studiato

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)

Malattie studiate

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)

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

Criteri di esclusione
- Previous bypass of the lesion to be treated. - Previous surgery within 30 days prior to the procedure in question. - Patient on dialysis. (BASEC)

Luogo dello studio

Lugano

(BASEC)

non disponibile

Sponsor

BIOTRONIK AG Ackerstrasse 6, 8180 Bülach, Switzerland

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Idir Hamdidouche

+41 75 429 5542

idir.hamdidouche@biotronik.com

BIOTRONIK AG Medical Affairs Ackerstrasse 6 | 8180 Bülach | Switzerland

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione d'etica Ticino

(BASEC)

Data di approvazione del comitato etico

28.07.2025

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
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)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
non disponibile

Intervento studiato
non disponibile

Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
non disponibile

non disponibile

Endpoint primari e secondari
non disponibile

non disponibile

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
non disponibile

Contatti aggiuntivi
non disponibile

ID secondari
non disponibile

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
non disponibile

Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile