NCT Number: NCT00343226
An Open, Randomized Pilot Study to Evaluate the Use of Basiliximab With an Optimized Cyclosporine Dosing on Renal Function in "de Novo" Liver Transplantation.
The objectives of the study are:To compare the renal function of a quadruple immunosuppressive regimen (including basiliximab in combination with an optimized cyclosporine dose during the first weeks post-transplantation, mycophenolate mofetil and corticosteroids) versus a standard triple therapy regimen (including cyclosporine standard dose, mycophenolate mofetil and corticosteroids)
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Notify MeKey information
Conditions
Age range
18 year–75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Who can participate
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- First cadaveric liver transplant
- ABO identical or compatible graft
Exclusion criteria
- Multiple organ transplant
- renal impairment defined as glomerular filtration rate (GFR) < 30 ml/min
- Fulminant liver failure
Other protocol-defined exclusion criteria may apply.
Treatment and study plan
Primary outcomes
-
Renal function (i.e. glomerular filtration rate) at 12 months post-transplantation
Secondary outcomes
-
Frequency and severity of rejection episodes before 6 and 12 months post-transplantation
-
Frequency of death, graft loss or retransplantation before 6 and 12 months post-transplantation
-
Adverse events
-
Duration of initial hospitalization and number or hospital re-admissions.
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Lead sponsor
Novartis
Industry
Registry information
Important dates
- Study start
- 2002
- Primary completion
- 2005
- First posted
- Jun 22, 2006
- Registry last updated
- Aug 25, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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