Nordic countries

About the ScanCLAD study

The purpose of the study is to evaluate whether the use of a once-daily tacrolimus-dose regimen (Advagraf®), based on anti-thymocyte globuline (Thymoglobulin®) induction, mycophenolate mofetil (MMF) and corticosteroids, reduces the cumulative incidence of CLAD after de novo lung transplantation at 36 months, in comparison with a twice-daily cyclosporin-based protocol, otherwise identical between groups. 

Study population is 242 male or female lung recipients 18-70 years of age undergoing primary double (including size reduction) lung transplantation (LTx), and who are willing and capable of giving written informed consent for study participation and anticipated to be able to participate in the study for 36 months.

Sponsor and Coordinating Investigator is Göran Dellgren, Consultant, PhD, Head of section for thorax transplantation l, Gothenburg, Sweden

Sahlgrenska University Hospital in Gothenburg, Sweden      Principal Investigator: Gerdt Riise, Consultant, Ass Prof, Head of section for lung transplantation

Skåne University Hospital in Lund, Sweden                     Principal Investigator: Johan Svahn, Consultant, PhD

Rigshospitalet in Copenhagen, Denmark                         Principal Investigator: Thomas Kromann Lund, Chief physician, PhD, Ass. Prof

Oslo University Hospital in Oslo, Norway                        Principal Investigator: Inga Leuckfeld, Consultant PhD

Helsinki University Hospital in Helsinki, Finland        Principal Investigator: Peter Raivio, M.D., D.Sc., Cardiothoracic Surgeon, Ass Prof

Recruitment graph