Initial Dosing of Paricalcitol in Secondary Hyperparathyroidism
Primary Purpose
Secondary Hyperparathyroidism
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
paricalcitol
Sponsored by
About this trial
This is an interventional treatment trial for Secondary Hyperparathyroidism focused on measuring hemodialysis; secondary hyperparathyroidism; hypercalcemia; hyperphosphatemia; vitamin D
Eligibility Criteria
Inclusion Criteria:-maintenance hemodialysis therapy (3 sessions per week) for at least 3 months; iPTH between 300 and 900 pg/mL; age > 18 years; normal serum calcium concentration (8.1 - 10.4 mg/dL); Ca x P product less than 70; no vitamin D metabolite replacement therapy for at least one month prior to the enrollment; aluminum levels lower than 60 μg/L. - Exclusion Criteria:administration of calcitonin, disphosphonates or corticosteroids; presence of a clinically serious medical condition; previous parathyroidectomy; active malignancy. -
Sites / Locations
Outcomes
Primary Outcome Measures
The primary outcome was the achievement of desired iPTH levels (150 - 300 pg/mL) in the two groups (iPTH/80 and iPTH/120).
Secondary Outcome Measures
The frequency of over-suppression of iPTH (< 150 pg/mL) was the secondary outcome.
Full Information
NCT ID
NCT00307840
First Posted
March 27, 2006
Last Updated
March 27, 2006
Sponsor
Papageorgiou General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00307840
Brief Title
Initial Dosing of Paricalcitol in Secondary Hyperparathyroidism
Official Title
Initial Dosing of Paricalcitol Based on iPTH Parathyroid Hormone Levels in Hemodialysis Patients With Secondary Hyperparathyroidism
Study Type
Interventional
2. Study Status
Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
February 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2005 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Papageorgiou General Hospital
4. Oversight
5. Study Description
Brief Summary
The purpose of this study was to compare two different initial dosing schemes for the administration of paricalcitol in hemodialysis patients with secondary hyperparathyroidism: the already in use iPTH/80 scheme, and an iPTH/120 scheme, which corresponds to the immediately lower dose, based on current instructions on paricalcitol dose adjustment. We studied the effectiveness of the two dosing schemes in achieving a target iPTH level (150 - 300 pg/mL)
Detailed Description
Adjustment of the initial dose of paricalcitol, in hemodialysis patients with secondary hyperparathyroidism (sHPT), on the basis of severity of sHPT is generally preferred in current practice. Whether the proposed dose, based on the formula baseline intact parathyroid hormone (iPTH [pg/mL]) divided by 80, is the most appropriate has not been adequately assessed. A trial comparing the iPTH/80 dose to the immediately lower iPTH/120 dose was undertaken. We studied the ability of the two different dosing schemes to control iPTH levels within a desired range between 150 and 300 pg/mL, as well as the frequency of iPTH over-suppression (< 150 pg/mL) in the two groups (iPTH/80 and iPTH/120).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Secondary Hyperparathyroidism
Keywords
hemodialysis; secondary hyperparathyroidism; hypercalcemia; hyperphosphatemia; vitamin D
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
paricalcitol
Primary Outcome Measure Information:
Title
The primary outcome was the achievement of desired iPTH levels (150 - 300 pg/mL) in the two groups (iPTH/80 and iPTH/120).
Secondary Outcome Measure Information:
Title
The frequency of over-suppression of iPTH (< 150 pg/mL) was the secondary outcome.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:-maintenance hemodialysis therapy (3 sessions per week) for at least 3 months; iPTH between 300 and 900 pg/mL; age > 18 years; normal serum calcium concentration (8.1 - 10.4 mg/dL); Ca x P product less than 70; no vitamin D metabolite replacement therapy for at least one month prior to the enrollment; aluminum levels lower than 60 μg/L.
-
Exclusion Criteria:administration of calcitonin, disphosphonates or corticosteroids; presence of a clinically serious medical condition; previous parathyroidectomy; active malignancy.
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Efstathios Mitsopoulos, MD
Organizational Affiliation
Papageorgiou General Hospital, Thessaloniki, Greece
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
11689389
Citation
Martin KJ, Gonzalez E, Lindberg JS, Taccetta C, Amdahl M, Malhotra K, Llach F. Paricalcitol dosing according to body weight or severity of hyperparathyroidism: a double-blind, multicenter, randomized study. Am J Kidney Dis. 2001 Nov;38(5 Suppl 5):S57-63. doi: 10.1053/ajkd.2001.28112.
Results Reference
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Initial Dosing of Paricalcitol in Secondary Hyperparathyroidism
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