Serum NGAL Levels in Hemodialysis (HD) Patients; Relation to Iron Status, HD and Intravenous (IV) Iron Administration
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|ClinicalTrials.gov Identifier: NCT00560976|
Recruitment Status : Unknown
Verified April 2013 by David Tovbin, Soroka University Medical Center.
Recruitment status was: Recruiting
First Posted : November 20, 2007
Last Update Posted : April 18, 2013
|Condition or disease||Intervention/treatment||Phase|
|Renal Failure Chronic Requiring Hemodialysis||Drug: Iron Saccharate (Venofer)||Not Applicable|
Serum and urine levels of the siderophore binding protein neutrophil gelatinase associated lipocalin (NGAL) are increased in a number of renal diseases, but has not been evaluated yet in dialysis patients. Since NGAL is suggested to be related to inflammatory processes and iron homeostasis, which are a major problem in dialysis patients, this study aims to assess the relation of serum NGAL levels in hemodialysis (HD) patients to iron status, inflammation, hemodialysis and intravenous(IV) iron administration. Our hypothesis is that serum NGAL levels in HD patients are related to iron status and inflammation and may change following hemodialysis and/or acute or chronic IV iron administration.
The Specific aims are:
- To assess the relations between basal serum NGAL levels to iron, dialysis, and inflammation related parameters.
- To assess the effect of HD on serum NGAL levels and their relation with with iron, dialysis and inflammation related parameters.
- To assess the effects of weekly 100 mg IV iron in the first hour of HD on serum NGAL levels, and the relation of pre IV iron serum NGAL levels with iron, oxidative stress and inflammation related parameters. These assessments will be performed in the first weekly HD.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||100 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Serum Neutrophil Gelatinase Associated Lipocalin (NGAL) Levels in Hemodialysis (HD) Patients; Relation to Iron Status, Hemodialysis, and Intravenous (IV) Iron Administration|
|Study Start Date :||December 2005|
|Estimated Primary Completion Date :||December 2014|
|Estimated Study Completion Date :||December 2014|
Experimental: Iron Saccharate (Venofer)
IV Iron Saccharate (Venofer)100 mg
Drug: Iron Saccharate (Venofer)
Hemodialysis with IV iron administration of 100 mg Iron Saccharate (Venofer) in 150 ml 0.9 % saline to the arterial dialysis line during first hour of mid-week dialysis session. An alternative IV iron brand in some centers participating in the study could bebe 62.5 mg ferric gluconate (Ferrlecit).
Other Name: Ferric gluconate (Ferrlecit)
- CRP (C-Reactive Protein) and AOPP (Advanced Oxidative Protein Products) Levels [ Time Frame: To assess the effects of 100 mg IV iron in the first hour of the first weekly HD on the relation of pre IV iron serum NGAL levels with oxidative stress and inflammation related parameters. ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00560976
|Contact: David Tovbin, MDemail@example.com|
|Department of Nephrology, Soroka University Medical center||Completed|
|Beer-Sheva, Israel, 84101|
|Bnai-zion Medical Center,Nephrology,||Completed|
|Department of Nephrology, Wolfson Medical Center||Recruiting|
|Contact: Alexander Biro, MD 97235028285 firstname.lastname@example.org|
|Contact: Katzir Zeev, MD 97235028291 Katzir@wolfson.health.gov.il|
|Principal Investigator: Alexander Biro, MD|
|Principal Investigator:||David Tovbin, MD||Soroka University Medical Center|