Comparison Between Effects of Two Iron Preparations on Protein in the Urine
Primary Purpose
Kidney Failure, Chronic, Anemia, Iron-Deficiency
Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
iron sucrose injection, USP
sodium ferric gluconate complex in sucrose injection
Sponsored by
About this trial
This is an interventional basic science trial for Kidney Failure, Chronic
Eligibility Criteria
Inclusion Criteria:
- Moderate to severe anemia
- Iron deficiency
- Moderate to severe chronic kidney disease, not receiving dialysis
- Age ≥ 18 or greater and able to give informed consent
Exclusion Criteria:
- Known sensitivity to Sodium Ferric Gluconate Complex in Sucrose Injection, Iron sucrose USP, or any of their components
- Clinically unstable
- Indication of iron sufficiency
- Bladder obstruction conditions that would not allow for good urine output
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Iron Sucrose
Ferric Gluconate
Arm Description
Outcomes
Primary Outcome Measures
Change in urine protein
Secondary Outcome Measures
Full Information
NCT ID
NCT00534144
First Posted
September 20, 2007
Last Updated
September 22, 2011
Sponsor
Watson Pharmaceuticals
1. Study Identification
Unique Protocol Identification Number
NCT00534144
Brief Title
Comparison Between Effects of Two Iron Preparations on Protein in the Urine
Official Title
A Randomized Controlled Trial of the Effect of IV Iron on Proteinuria in Non-Dialysis Chronic Kidney Disease Patients
Study Type
Interventional
2. Study Status
Record Verification Date
September 2011
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
November 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Watson Pharmaceuticals
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will compare the effects of sodium ferric gluconate complex and iron sucrose on urine concentrations of various chemicals including protein
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Failure, Chronic, Anemia, Iron-Deficiency
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
74 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Iron Sucrose
Arm Type
Active Comparator
Arm Title
Ferric Gluconate
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
iron sucrose injection, USP
Intervention Description
iron sucrose injection, USP, 100 mg intravenously (IV) per week, for 5 weeks
Intervention Type
Drug
Intervention Name(s)
sodium ferric gluconate complex in sucrose injection
Intervention Description
sodium ferric gluconate complex in sucrose injection, 100 mg intravenously (IV) per week, for 5 weeks
Primary Outcome Measure Information:
Title
Change in urine protein
Time Frame
6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Moderate to severe anemia
Iron deficiency
Moderate to severe chronic kidney disease, not receiving dialysis
Age ≥ 18 or greater and able to give informed consent
Exclusion Criteria:
Known sensitivity to Sodium Ferric Gluconate Complex in Sucrose Injection, Iron sucrose USP, or any of their components
Clinically unstable
Indication of iron sufficiency
Bladder obstruction conditions that would not allow for good urine output
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Naomi V. Dahl, Pharm.D.
Organizational Affiliation
Watson Laboratories, Inc.
Official's Role
Study Director
Facility Information:
City
Phoenix
State/Province
Arizona
Country
United States
City
Alhambra
State/Province
California
Country
United States
City
Bell Gardens
State/Province
California
Country
United States
City
Exeter
State/Province
California
Country
United States
City
Glendale
State/Province
California
Country
United States
City
Visalia
State/Province
California
Country
United States
City
Ft Lauderdale
State/Province
Florida
Country
United States
City
Hines
State/Province
Illinois
Country
United States
City
Shreveport
State/Province
Louisiana
Country
United States
City
Boston
State/Province
Massachusetts
Country
United States
City
Houston
State/Province
Texas
Country
United States
City
Fairfax
State/Province
Virginia
Country
United States
City
San Juan
Country
Puerto Rico
12. IPD Sharing Statement
Citations:
PubMed Identifier
20876669
Citation
Agarwal R, Leehey DJ, Olsen SM, Dahl NV. Proteinuria induced by parenteral iron in chronic kidney disease--a comparative randomized controlled trial. Clin J Am Soc Nephrol. 2011 Jan;6(1):114-21. doi: 10.2215/CJN.06020710. Epub 2010 Sep 28.
Results Reference
result
Learn more about this trial
Comparison Between Effects of Two Iron Preparations on Protein in the Urine
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