NCT Number: NCT00189501
A Multi-Center, Observational Registry of Subjects With Secondary Hyperparathyroidism (HPT) and Chronic Kidney Disease (CKD)
Objectives include description of current practices; assessment over time of K/DOQI goals, clinical outcomes, health resource utilization(HRU) and patient reported outcomes (PRO) and the impact of Sensipar® on these parameters
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- 3 month history of Stage 4 or Stage 5 CKD
- A PTH value within 3 months of enrollment
- If relevant, completion of Sensipar® study prior to enrolling in Registry Exclusion Criteria:
- Females who are pregnant or breast feeding
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Amgen
Industry
Registry information
Important dates
- Study start
- 2004
- First posted
- Sep 19, 2005
- Registry last updated
- Dec 28, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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