WHO ICTRP trial

Multicentre, prospective, randomized, open-label, controlled study in de novo…

EUCTR2007-005844-26-BE · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2007-005844-26-BE
Public title Multicentre, prospective, randomized, open-label, controlled study in de novo kidney transplant recipients to evaluate the impact of cyclosporine or steroid withdrawal at 3 months on graft function, patient and graft survival, and cardiovascular surrogate markers during the first five years after transplantation. - Cistcert
Scientific title Multicentre, prospective, randomized, open-label, controlled study in de novo kidney transplant recipients to evaluate the impact of cyclosporine or steroid withdrawal at 3 months on graft function, patient and graft survival, and cardiovascular surrogate markers during the first five years after…
Primary sponsor Antwerp University Hospital
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes
Countries Belgium
Conditions Preservation of renal function after kidney transplantation in a 5-year, multicentre, prospective, randomized, open-label, controlled study Patients will be randomized within 24 hours prior to transplantation. ? Group 1: Simulect + Neoral +…
Interventions Trade Name: Certican 0.25 mg Pharmaceutical Form: Tablet INN or Proposed INN: EVEROLIMUS CAS Number: 159351696 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 0.25- Trade Name: Certican 0.50 mg…
Registration date Apr 25, 2008
Secondary IDs Cistcert
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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