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NCT03106298 · ClinicalTrials.gov registry record

Iron Deficiency and FGF23 Regulation in CKD and HF

A clinical trial of Chronic Kidney Diseases and Iron Deficiency Anemia, sponsored by Northwestern University.

Completed
Registry status
77
Enrollment target
1
Study location

NCT03106298 is a study of Chronic Kidney Diseases and Iron Deficiency Anemia that has completed, run by Northwestern University. The registered enrollment target is 77 participants, below the 444-participant average among 73 other Chronic Kidney Diseases trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03106298, a study of Chronic Kidney Diseases and Iron Deficiency Anemia, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
77 participants
Enrollment target
1
Study location

Study Summary

This study investigates the effects of intravenous (IV) iron sucrose therapy on blood levels of Fibroblast Growth Factor 23 (FGF23, a protein that regulates the amount of phosphate in the body) in iron deficiency anemia in healthy participants, participants with Congestive Heart Failure (CHF, where the heart does not pump adequate blood supply to the body), participants with Chronic Kidney Disease (CKD, where the kidney function is reduced), and participants with CKD and CHF.

Interventions

  • DRUG Iron Sucrose

Study Locations (1)

Illinois

  • Northwestern University - Chicago

Trial Details

FieldValue
Enrollment Target 77 participants
Start Date 2015-12-18
Est. Completion 2018-08-01

Sponsor

Northwestern University

1,209 total trials

What the Registry Record Tells You About NCT03106298

The ClinicalTrials.gov registry entry for NCT03106298 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 77 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 444-participant average among 73 other Chronic Kidney Diseases trials with a reported enrollment target (83% lower). The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Chronic Kidney Diseases appearing as the primary indexed condition, and to 1 intervention - of which Iron Sucrose is the first listed.

NCT03106298 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT03106298 about?

NCT03106298 is a clinical study titled "Iron Deficiency and FGF23 Regulation in CKD and HF". This study investigates the effects of intravenous (IV) iron sucrose therapy on blood levels of Fibroblast Growth Factor 23 (FGF23, a protein that regulates the amount of phosphate in the body) in iron deficiency anemia in healthy participants, participants with Congestive Heart Failure (CHF, where ...

What is the current status of trial NCT03106298?

This trial is currently completed. The enrollment target is 77 participants. The study started on 2015-12-18. Estimated completion is 2018-08-01.

What conditions does trial NCT03106298 study?

This clinical trial studies the following conditions: Chronic Kidney Diseases, Iron Deficiency Anemia, Chronic Heart Failure.

What interventions are being tested in trial NCT03106298?

The interventions under investigation include: Iron Sucrose (DRUG).

Who is sponsoring clinical trial NCT03106298?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03106298 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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