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Completed Phase 2 Interventional Results available

Dose Ranging Study of Dialysate Containing Soluble Iron to Treat Subjects With End Stage Renal Disease (ESRD) Receiving Chronic Hemodialysis

ClinicalTrials.gov ID: NCT00548249

Public ClinicalTrials.gov record NCT00548249. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 1:23 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Dose Ranging Study of Dialysate Containing Soluble Ferric Pyrophosphate (SFP) Versus Control in Subjects With ESRD Receiving Chronic Hemodialysis.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether Dialysate containing soluble iron (Soluble Ferric Pyrophosphate) is safe and effective in maintaining physiological iron levels during chronic hemodialysis.

Study identification

NCT ID
NCT00548249
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
131 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2007
Primary completion
Sep 30, 2009
Completion
Dec 31, 2009
Last update posted
Dec 1, 2020

2007 – 2010

United States locations

U.S. sites
27
U.S. states
17
U.S. cities
27
Facility City State ZIP Site status
Investigator Tempe Arizona 85284
Investigator Hacienda Heights California 91745
Investigator Los Angeles California 90059
Investigator Whittier California 90603
Investigative Site Augusta Georgia 30901
Investigator Meridian Idaho 83642
Investigator Chicago Illinois 60617
Investigative Site Louisville Kentucky 40202-1718
Investigator New Orleans Louisiana 70115
Investigator Springfield Massachusetts 01107
Investigative Site Detroit Michigan 48202
Investigator Hackensack New Jersey 07601
Investigator Brooklyn New York 11212
Investigator Great Neck New York 11021
Investigator Mineola New York 11501
Investigator New York New York 10013
Investigator Ridgewood New York 11385
Investigator Winston-Salem North Carolina 27103
Investigative Site Canton Ohio 44718
Investigator Cincinnati Ohio 45229
Investigative Site Hershey Pennsylvania 17033
Investigator Arlington Texas 76011
Investigator Fort Worth Texas 76105
Investigator McAllen Texas 78503
Investigator San Antonio Texas 78207
Investigator Arlington Virginia 22206
Investigator Seattle Washington 92133

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00548249, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 1, 2020 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00548249 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →