Tryptik Ti Study

• Research type

  Research Study

• Full title

  Prospective evaluation of clinical and radiographic outcomes after Anterior Cervical interbody fusion surgery using a TRYPTIK® Ti-Life cage.

• IRAS ID

  301656

• Contact name

  Dervilla Bermingham

• Contact email

  dbermingham@spineart.com

• Sponsor organisation

  Spineart SA

• ISRCTN Number

  ISRCTN63972735

• Duration of Study in the UK

  3 years, 0 months, 1 days

• Research summary

  This study is a prospective, interventional, single-arm, multicenter study on patients receiving Anterior Cervical Discectomy with Fusion (ACDF) surgery for degenerative disk diseases (DDD) with at least one and up to 4 TRYPTIK® TI cervical cages. The purpose is to evaluate mid- and long-term clinical and radiographic outcomes.

• REC name

  West of Scotland REC 4

• REC reference

  21/WS/0155

• Date of REC Opinion

  11 Mar 2022

• REC opinion

  Further Information Favourable Opinion