Secondary Hyperparathyroidism Clinical Trial
Official title:
A Retrospective Evaluation of Sensipar Use in Renal Transplant Recipients
Verified date | December 2007 |
Source | Amgen |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
Retrospective chart review to gather information on Sensipar patterns of use and effects on biochemical parameters in renal transplant recipients
Status | Completed |
Enrollment | 50 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Adults >= 18 years old - Subjects who have received Sensipar for a duration of at least 3 months, beginning at least 3 months after a kidney transplant. Subjects must have begun Sensipar teatment no later than Februry 28, 2005 at treating physician's discretion. Exclusion Criteria: - Subjects who received Sensipar before undergoing a kidney transplant - Subjects receiving dialysis post-transplant |
Time Perspective: Retrospective
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Amgen |
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