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Clinical Trials/IRCT138904263325N3
IRCT138904263325N3Completed未知

Effect of short-term and low amount of intravenous Ascorbic Acid on reducing ferritin in Hemodialysis Patients without increasing the start dosage of erythropoietin: crossed over double blind randomized controlled trial

Zanjan University of Medical Sciences0 sites30 target enrollmentStarted: TBDLast updated:
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Conditions

Trial Snapshot

Phase
未知
Status
Completed
Enrollment
30
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
no limit to no limit (—)
Sex
All

Inclusion Criteria

  • •receiving hemodialysis therapy for at least 6 months, administered EPO for 6 months or longer at a dose of 80-360 U/kg/wk or greater, rolling 3-month average Hb level of 11.0 g/dL or less (110 g/L), ferritin level greater than 500 ng/Ml, transferrin saturation (TSAT) of 20% or less and administered maintenance intravenous iron (25-100 mg/week)
  • •Exclusion criteria: bone marrow malignancy, myelodysplastic syndrome, evidence of chronic infection, hemochromatosis, hemoglobinopathies, evidence of significant bleeding (decrease in Hb level = 2 g/dL during the past 3 months, mean corpuscular volume greater than 100 fL, biointact parathyroid hormone (bio-PTH) level greater than 500 pg/mL (ng/L)

Exclusion Criteria

  • Not provided

Investigators

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