Post Transplant Study

Completed

• Conditions: Kidney Tansplant; Secondary Hyperparathyroidism; Hyperparathyroidism

• Registration Number: NCT00395902
• Lead Sponsor: Amgen

Brief Summary

Retrospective chart review to gather information on Sensipar patterns of use and effects on biochemical parameters in renal transplant recipients

Detailed Description

Not available

Study Timeline

• Study Start: 2005-08
• Study First Submitted: 2006-11-02
• Study First Submitted QC: 2006-11-02
• Study First Posted: 2006-11-06
• Status Verified: 2007-12
• Last Update Submitted: 2007-12-20
• Last Update Posted: 2007-12-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified