Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01149993

Attenuating Ischemia Reperfusion Injury After Living Donor Renal Transplantation

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Georgetown University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Patients undergoing living donor renal transplant will be asked to participate to determine whether pre-operative dosing of immunosuppressive medication, and the donor organ receiving an additional dose of antibody induction therapy helps to alleviate potential damage to the transplanted organ post-transplant. A number of lab tests will be done post-transplant to determine how well the kidney is functioning.

Conditions

Interventions

TypeNameDescription
DRUGMyfortic (mycophenolic acid)720mg twice a day for 7 days prior to transplantation
DRUGMyfortic (mycophenolic acid)720mg twice a day after transplant
DRUGThymoglobulin (anti-thymocyte globulin)up to 25 mg will be infused into the renal artery of a donor kidney prior to transplantation into the recipient.
DRUGThymoglobulin (anti-thymocyte globulin)standard of care for Georgetown University Hospital: 1.5 mg/kg/day infused over 6 hours.

Timeline

Start date
2010-06-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2010-06-24
Last updated
2014-06-09

Source: ClinicalTrials.gov record NCT01149993. Inclusion in this directory is not an endorsement.