- CSR Summary Not Available
- NCT00816166
- Primary Citation
- Data Specification Not Available
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Trial Information
Generic NameN/AProduct NameVitesse Intracranial StentTherapeutic AreaNervous System DiseasesEnrollment125% Female34.2%% White72%
Product ClassNeurovascular deviceSponsor Protocol NumberVISSIT CA-2007-01Data PartnerJohnson & JohnsonCondition StudiedIschemic StrokeMean/Median Age (Years)61.8
Supporting Documentation
- Collected Datasets Available
- Protocol with Amendments Available
Approved Data Requests Associated with this Trial
- 2024-0740 : Prognostic Enrichment Efficiency Ratio
- 2024-0580 : Developing approaches to accelerate clinical trials using real world data (RWD) from electronic health records (EHR)
- 2023-5534 : Quality tolerance limit and duplicated patient investigation in clinical trials
- 2022-5100 : Identification of Patients Who Can Benefit from Intracranial Stent Placement: analysis of Vitesse Intracranial Stent Study for Ischemic Stroke Therapy