Post Transplant Study
This study has been completed.
Sponsor:
Amgen
Information provided by:
Amgen
ClinicalTrials.gov Identifier:
NCT00395902
First received: November 2, 2006
Last updated: December 20, 2007
Last verified: December 2007
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Purpose
Retrospective chart review to gather information on Sensipar patterns of use and effects on biochemical parameters in renal transplant recipients
| Condition | Intervention |
|---|---|
|
Kidney Tansplant Secondary Hyperparathyroidism Hyperparathyroidism |
Drug: Sensipar after Post Transplant |
| Study Type: | Observational |
| Study Design: | Time Perspective: Retrospective |
| Official Title: | A Retrospective Evaluation of Sensipar Use in Renal Transplant Recipients |
Resource links provided by NLM:
Further study details as provided by Amgen:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
Criteria
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
Contacts and Locations
More Information
Additional Information:
No publications provided
| Responsible Party: | Global Development Leader, Amgen Inc. |
| ClinicalTrials.gov Identifier: | NCT00395902 History of Changes |
| Other Study ID Numbers: | 20040261, 2004261 |
| Study First Received: | November 2, 2006 |
| Last Updated: | December 20, 2007 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Amgen:
|
Sensipar cinacalcet Mimpara |
Additional relevant MeSH terms:
|
Hyperparathyroidism Hyperparathyroidism, Secondary Parathyroid Diseases Endocrine System Diseases |
ClinicalTrials.gov processed this record on May 16, 2013