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Clinical Trial Summary

The safety and preliminary efficacy of the addition of an aqueous curcumin-cyclodextrin complex (CDC) solution to graft perfusion solution is studied. CDC has proved safe and highly effective in preventing primary graft non-function, delayed graft function and chronic dysfunction in pre-clinical kidney transplantation animal models. The hypothesis is that addition of CDC to the graft perfusion solution will decrease the incidence of delayed graft function in human kidney transplantation subjects.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01285375
Study type Interventional
Source Helsinki University Central Hospital
Contact Jakob Stenman, MD, PhD
Phone +35894711
Email jakob.stenman@hus.fi
Status Recruiting
Phase Phase 1
Start date January 2011
Completion date December 2012

See also
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Terminated NCT01609673 - Study of Everolimus in de Novo Renal Transplant Recipients N/A
Active, not recruiting NCT01413464 - The Risk of Venous Clotting in Patients After Renal Transplant N/A
Completed NCT01653847 - Study in Recipients of Renal Transplant Allograft to Evaluate the Impact of Two Immunosuppressive Regimens N/A