- 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