Sickle Cell Disease Clinical Trial
Official title:
Kidney Transplantation in Patients With Sickle Cell Disease
Verified date | February 2013 |
Source | Emory University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
The purpose of this research is to better characterize the components and mechanisms of the immune systems of persons with sickle cell disease who have had a kidney transplant and are immunosuppressed. If we can improve our scientific understanding of the fundamental mechanisms involved in patient outcomes, we can potentially maximize the benefits that we seek from transplantation in sickle cell patients with end stage renal disease.
Status | Terminated |
Enrollment | 2 |
Est. completion date | December 2010 |
Est. primary completion date | December 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Male or female patients between 18 and 65 years of age 2. Patients capable of understanding the purposes and risks of the study, who can give written informed consent and who are willing to participate in and comply with the study. 3. Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to enrollment and must not be breast-feeding. 4. Patients must be diagnosed with Sickle Cell Disease (SS phenotype) Exclusion Criteria: 1. Patients with any prior organ transplant or multi-organ transplant recipients. 2. Patients with evidence of an active systemic infection requiring the continued use of antibiotics, evidence of an HIV infection, or the presence of a chronic active hepatitis B or C. 3. Patients with history of malignancy in the last 5 years (except successfully treated localized non-melanotic skin cancer) 4. Patients with active illegal drug use |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Mason Outpatient Tranplant Clinic Emory University | Atlanta | Georgia |
Lead Sponsor | Collaborator |
---|---|
Emory University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | No measure applied | One 12 month participant, with no actions. One subject was a screen failure due to hepatitis C. | 05/08/2008-6/05/2009 | No |
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