Intracranial Stenosis Clinical Trial
Official title:
AcandiS Stenting of Intracranial STENosis - regisTry
ASSISTENT is designed to collect comprehensive information on technical and clinical safety of the use of Credo® stent together with the NeuroSpeed® PTA balloon catheter in clinical practice in an open registry.
ASSISTENT is subdivided into two components. The first part only requires recording of data acquired in routine clinical practice during the treatment of patients with intracranial stenosis with the self-expandable Credo® stent until discharge. This comprises demographic data, data concerning the qualifying clinical event, limited data on medical history and medication, information about the intervention including technical success and periprocedural complications or events, and information about events and clinical status during the in-hospital treatment until hospital discharge. The second part of the registry consists of a follow-up visit 30 days after the interventional procedure which will be conducted outside of clinical practice. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Enrolling by invitation |
NCT05583305 -
Prevalence and Etiologies of Intracranial Stenosis in Patients With Antiphospholipid Syndrome
|
||
| Not yet recruiting |
NCT05270746 -
The Predictive Value of Retinal Vascular Signs for Intracranial Artery Stenosis (RVS-ICAS)
|
||
| Active, not recruiting |
NCT05403593 -
Registry of Emergent Large veSsel oCclUsion duE to IntraCranial AtherosclerosiS
|
||
| Terminated |
NCT03955835 -
Acandis Credo Intracranial Stent for Unsuccessful Recanalization After Thrombectomy (ACUTE)
|
N/A | |
| Completed |
NCT02506907 -
Characterizing Hemodynamic Compensation in Patients With Intracranial Stenosis
|
N/A |