Ailliance Study

• Research type

  Research Study

• Full title

  The Ailliance Post-Market Clinical Study: All enablIng technoLogies, bioLogics, IDS, And core spiNe produCt collEction

• IRAS ID

  346104

• Contact name

  Bart Heijen

• Contact email

  bart.heijnen@medtronic.com

• Sponsor organisation

  Medtronic

• Clinicaltrials.gov Identifier

  NCT05856370

• Duration of Study in the UK

  4 years, 11 months, 30 days

• Research summary

  The purpose of this study is to gather information about the safety and performance of commercially available Medtronic Cranial and Spinal Technology devices. This information will be used to evaluate the devices and make sure that they still meet regulatory requirements. The information will also be used to improve current devices and develop future devices and treatments.

• REC name

  London - Stanmore Research Ethics Committee

• REC reference

  25/LO/0229

• Date of REC Opinion

  17 Jul 2025

• REC opinion

  Further Information Favourable Opinion