VISTA

• Research type

  Research Study

• Full title

  VISTA: Navitor Post-Market Clinical Follow Up Study

• IRAS ID

  333656

• Contact name

  Rebecca Malpass

• Contact email

  rebecca.malpass@abbott.com

• Clinicaltrials.gov Identifier

  NCT00000000

• Duration of Study in the UK

  5 years, 7 months, 30 days

• Research summary

  This purpose of this study is to collect medical information and experiences related to the Navitor TAVI system (Navitor valve, Navitor loading system, and FlexNav delivery system). The Navitor TAVI system has been approved for use in the UK, and this study will collect additional information to better understand how the device performs in the real world.

• REC name

  HSC REC B

• REC reference

  23/NI/0135

• Date of REC Opinion

  10 Nov 2023

• REC opinion

  Further Information Favourable Opinion