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NCT01555060 · ClinicalTrials.gov registry record · Phase 2

Hemoglobin and Iron Recovery Study

A Phase 2 study, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

Completed
Registry status
Phase 2
Development phase
215
Enrollment target

NCT01555060 is a Phase 2 study that has completed, run by National Heart, Lung, and Blood Institute (NHLBI). The registered enrollment target is 215 participants.

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The verdict

NCT01555060, a Phase 2 study, has completed, sponsored by National Heart, Lung, and Blood Institute (NHLBI).

COMPLETED
Registry status
Phase 2
Development phase
215 participants
Enrollment target

Study Summary

The purpose of this study is to investigate the effect of daily iron supplements after blood donation on time to recovery of hemoglobin and iron stores. The study will also determine whether the effect of iron supplements on time to recovery is different in men and women, in older vs. younger donors (\<60 years old vs. at least 60 years old) and in donors with replete vs. diminished pre-donation iron stores.

Interventions

  • DIETARY_SUPPLEMENT ferrous gluconate

Trial Details

FieldValue
Enrollment Target 215 participants
Start Date 2012-03
Est. Completion 2013-06
Phase Phase 2

What the Registry Record Tells You About NCT01555060

The ClinicalTrials.gov registry entry for NCT01555060 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 215 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Heart, Lung, and Blood Institute (NHLBI), which has 501 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which ferrous gluconate is the first listed.

NCT01555060 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01555060 about?

NCT01555060 is a clinical study titled "Hemoglobin and Iron Recovery Study". The purpose of this study is to investigate the effect of daily iron supplements after blood donation on time to recovery of hemoglobin and iron stores. The study will also determine whether the effect of iron supplements on time to recovery is different in men and women, in older vs. younger donors...

What is the current status of trial NCT01555060?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 215 participants. The study started on 2012-03. Estimated completion is 2013-06.

What interventions are being tested in trial NCT01555060?

The interventions under investigation include: ferrous gluconate (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT01555060?

This trial is sponsored by National Heart, Lung, and Blood Institute (NHLBI), which has 501 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.