|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | Abbott |
|---|---|
| Information provided by: | Abbott |
| ClinicalTrials.gov Identifier: | NCT00048516 |
Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Renal Insufficiency, Chronic |
Drug: paricalcitol capsule |
Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic Kidney Disease Subjects (Daily Dosing) |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
If female:
For entry into Pretreatment Phase:
For entry into Treatment Phase:
Exclusion Criteria:
Contacts and Locations| United States, California | |
| VA Greater Los Angeles Healthcare System, West Los Angeles | |
| Los Angeles, California, United States, 90073 | |
| Nephrology Associates Medical Group | |
| Riverside, California, United States, 92501 | |
| Kidney Center, Inc. | |
| Simi Valley, California, United States, 93065 | |
| United States, Colorado | |
| Denver Nephrologists | |
| Denver, Colorado, United States, 80220 | |
| University of CO Health Sciences Center | |
| Denver, Colorado, United States, 80262 | |
| United States, Iowa | |
| Dialysis PC | |
| Des Moines, Iowa, United States, 50309 | |
| United States, Minnesota | |
| Twin Cities Clinical Research | |
| Arden Hills, Minnesota, United States, 55126 | |
| United States, New York | |
| Long Island College Hospital | |
| Brooklyn, New York, United States, 11201 | |
| Erie County Medical Center | |
| Buffalo, New York, United States, 14215 | |
| United States, Pennsylvania | |
| Temple University Hospital | |
| Philadelphia, Pennsylvania, United States, 19140 | |
| United States, South Carolina | |
| Medical University of South Carolina | |
| Charleston, South Carolina, United States, 29425 | |
| United States, South Dakota | |
| Avera McKennan Research Institute | |
| Sioux Falls, South Dakota, United States, 57105 | |
| United States, Tennessee | |
| Nephrology Associates | |
| Nashville, Tennessee, United States, 37205 | |
| United States, Texas | |
| San Antonio Kidney Disease Research Center | |
| San Antonio, Texas, United States, 78219 | |
| United States, Virginia | |
| Clinical Research Associates of Tidewater | |
| Norfolk, Virginia, United States, 23507 | |
| United States, Washington | |
| FHS Research Center | |
| Tacoma, Washington, United States, 98405 | |
| Poland | |
| Wojewodzki Szpital Specjalistyczny AM w Bialymstoku | |
| Bialymstoku, Poland | |
| Krakow Hospital | |
| Krakow, Poland | |
| Study Director: | Laura Williams, M.D. | Abbott |
More Information
| ClinicalTrials.gov Identifier: | NCT00048516 History of Changes |
| Other Study ID Numbers: | 2001-021 |
| Study First Received: | November 1, 2002 |
| Last Updated: | July 31, 2006 |
| Health Authority: | United States: Food and Drug Administration |
|
Kidney Diseases Kidney Failure, Chronic Renal Insufficiency, Chronic Renal Insufficiency Urologic Diseases |