CELTIC
Research type
Research Study
Full title
Celtic Bifurcation Study A randomized multicentre trial to compare outcomes for patients with ischaemic heart disease and bifurcation coronary artery lesions who are treated with Xiences or Synergy stents
IRAS ID
163144
Contact name
Simon WALSH
Contact email
Sponsor organisation
CERIC
Clinicaltrials.gov Identifier
Duration of Study in the UK
3 years, 2 months, 17 days
Research summary
Randomized, prospective, post-market, multicenter study performed in two countries where Synergy II and Xience Xpedition stents are CE approved. One hundred and seventy (170) consecutive patients are planned to be enrolled in up to nine participating investigational sites.
REC name
HSC REC A
REC reference
14/NI/1114
Date of REC Opinion
6 Nov 2014
REC opinion
Further Information Favourable Opinion