Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DRUG | Myfortic (mycophenolic acid) | 720mg twice a day for 7 days prior to transplantation |
| DRUG | Myfortic (mycophenolic acid) | 720mg twice a day after transplant |
| DRUG | Thymoglobulin (anti-thymocyte globulin) | up to 25 mg will be infused into the renal artery of a donor kidney prior to transplantation into the recipient. |
| DRUG | Thymoglobulin (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.