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| Tracking Information | |||||
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| First Received Date ICMJE | November 1, 2002 | ||||
| Last Updated Date | July 31, 2006 | ||||
| Start Date ICMJE | February 2002 | ||||
| Primary Completion Date | |||||
| Current Primary Outcome Measures ICMJE |
The efficacy endpoint is achievement of two consecutive > or = 30% decreases from baseline in iPTH levels | ||||
| Original Primary Outcome Measures ICMJE |
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| Change History | Complete list of historical versions of study NCT00048516 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE | |||||
| Original Secondary Outcome Measures ICMJE | |||||
| Descriptive Information | |||||
| Brief Title ICMJE | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic Kidney Disease Subjects (Daily Dosing) | ||||
| Official Title ICMJE | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic Kidney Disease Subjects (Daily Dosing) | ||||
| Brief Summary | The objective of this study is to determine whether paricalcitol is safe and effective compared to placebo in reducing elevated serum PTH levels in patients with chronic kidney disease. |
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| Detailed Description | |||||
| Study Phase | Phase III | ||||
| Study Type ICMJE | Interventional | ||||
| Study Design ICMJE | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study | ||||
| Condition ICMJE | Renal Insufficiency, Chronic | ||||
| Intervention ICMJE | Drug: paricalcitol capsule | ||||
| Study Arms / Comparison Groups | |||||
| Publications * | |||||
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 68 | ||||
| Completion Date | |||||
| Primary Completion Date | |||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States, Poland | ||||
| Administrative Information | |||||
| NCT ID ICMJE | NCT00048516 | ||||
| Responsible Party | |||||
| Study ID Numbers ICMJE | 2001-021 | ||||
| Study Sponsor ICMJE | Abbott | ||||
| Collaborators ICMJE | |||||
| Investigators ICMJE |
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| Information Provided By | Abbott | ||||
| Verification Date | July 2006 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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