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Endovenous Versus Liposomal Iron in CKD

Primary Purpose

Iron Deficiency Anemia, Chronic Kidney Disease

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
gluconate iron
Liposomal iron
Sponsored by
Federico II University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Iron Deficiency Anemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years;
  • Signed written informed consent;
  • Glomerular filtration rate (GFR) ≤ 60 mL/min (MDRD GFR calculated according to 4 variables);
  • hemoglobin ≤ 12g/dL;
  • Ferritin ≤ 100ng/mL with transferrin saturation (TSAT) ≤ 25%;
  • If erythropoiesis stimulating agents (ESA) therapy, stable dose for at least three months;

Exclusion Criteria:

  • Infectious diseases;
  • bleeding in the preceding six months;
  • History of malignancy tumor in the last 3 years;
  • Anemia case different from that resulting from CKD;
  • vitamin B12 and folate deficiency;
  • Surgery of any kind in the last three months;
  • systemic haematological disease;
  • Blood Transfusions, therapy with intravenous or oral iron in the last three months;
  • Severe liver disease / test positive for hepatitis C virus (HCV) and hepatitis B virus (HBV);
  • Abuse of alcohol and drugs in the preceding six months;
  • immunosuppressive therapy ;
  • Significant weight loss;
  • Pregnancy or breast-feeding.

Sites / Locations

  • Federico II University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

oral liposomal iron

endovenous iron

Arm Description

patients receive a dose of liposomal 30 mg/die iron (equivalent to 1 cp Sideral forte).

patients receive a total dose 1000 mg of intravenous iron gluconate divided into administrations of 125 mg diluted in 250 mL normal saline infused weekly for 3 months

Outcomes

Primary Outcome Measures

modification in hemoglobin levels

Secondary Outcome Measures

Full Information

First Posted
May 24, 2013
Last Updated
July 23, 2014
Sponsor
Federico II University
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1. Study Identification

Unique Protocol Identification Number
NCT01864161
Brief Title
Endovenous Versus Liposomal Iron in CKD
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federico II University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Anemia is a common complication in patients with chronic kidney disease (CKD). In addition to erythropoietin deficiency, many studies have identified iron deficiency as a cause of anemia in CKD patients. Most patients with CKD are iron deficient because of: inadequate intake and absorption, gastroenteric bleeding, urinary iron loss in patient with significant proteinuria. The iron treatment is pivotal to manage anemic patients with CKD: the prescription of iron is usually oral because of practicality and safety, but often it is inevitable to administer intravenous iron because of gastroenteric malabsorption, intolerance to oral administration, irregular intake. There're few randomized controlled studies about the efficacy of oral iron versus intravenous iron in patients not on dialysis; most of them demonstrate superiority of intravenous therapy to restore iron deficiency and hemoglobin levels. A particular formulation of iron, liposomal iron has a high gastroenteric absorption and high bioavailability with lower incidence of side effects. The investigators study aims to evaluate the efficacy of treatment with liposomal oral iron compared to intravenous iron in CKD anemic patients not on dialysis in the presence of iron deficiency.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Iron Deficiency Anemia, Chronic Kidney Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
oral liposomal iron
Arm Type
Experimental
Arm Description
patients receive a dose of liposomal 30 mg/die iron (equivalent to 1 cp Sideral forte).
Arm Title
endovenous iron
Arm Type
Active Comparator
Arm Description
patients receive a total dose 1000 mg of intravenous iron gluconate divided into administrations of 125 mg diluted in 250 mL normal saline infused weekly for 3 months
Intervention Type
Drug
Intervention Name(s)
gluconate iron
Other Intervention Name(s)
FERLIXIT
Intervention Description
FERLIXIT fl 15mg/kg divided into weekly administrations of 125mg up to a maximum of 1000mg
Intervention Type
Drug
Intervention Name(s)
Liposomal iron
Other Intervention Name(s)
Sideral forte
Intervention Description
Sideral forte 30 mg/die
Primary Outcome Measure Information:
Title
modification in hemoglobin levels
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years; Signed written informed consent; Glomerular filtration rate (GFR) ≤ 60 mL/min (MDRD GFR calculated according to 4 variables); hemoglobin ≤ 12g/dL; Ferritin ≤ 100ng/mL with transferrin saturation (TSAT) ≤ 25%; If erythropoiesis stimulating agents (ESA) therapy, stable dose for at least three months; Exclusion Criteria: Infectious diseases; bleeding in the preceding six months; History of malignancy tumor in the last 3 years; Anemia case different from that resulting from CKD; vitamin B12 and folate deficiency; Surgery of any kind in the last three months; systemic haematological disease; Blood Transfusions, therapy with intravenous or oral iron in the last three months; Severe liver disease / test positive for hepatitis C virus (HCV) and hepatitis B virus (HBV); Abuse of alcohol and drugs in the preceding six months; immunosuppressive therapy ; Significant weight loss; Pregnancy or breast-feeding.
Facility Information:
Facility Name
Federico II University
City
Naples
ZIP/Postal Code
80131
Country
Italy

12. IPD Sharing Statement

Learn more about this trial

Endovenous Versus Liposomal Iron in CKD

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