RecruitingPhase 3NCT05304442

IV Iron Trial for Anemia Related to Uterine Bleeding in Female Patients Presenting to the Emergency Department

Intravenous Ferric Derisomaltose for Moderate to Severe Anemia Due to Uterine Bleeding in the Emergency Department: a Randomized Trial


Sponsor

Baylor College of Medicine

Enrollment

40 participants

Start Date

Sep 15, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

The primary aim of this randomized trial is to assess the efficacy of IV Ferric Derisomaltose vs Oral Iron in the management of women with severe Iron Deficiency Anemia due to Uterine Bleeding in the emergency department.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Ferric Derisomaltose 1000 Mg in 10 mL INTRAVENOUS SOLUTION [Monoferric] and a drug called Ferrous Sulfate 65 mg elemental iron (325 mg tablets) for people with anemia, iron deficiency and uterine bleeding. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGFerric Derisomaltose 1000 Mg in 10 mL INTRAVENOUS SOLUTION [Monoferric]

Single Dose of IV Iron

DRUGFerrous Sulfate 65 mg elemental iron (325 mg tablets)

Once daily by mouth for 42 days


Locations(1)

Ben Taub Hospital

Houston, Texas, United States

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NCT05304442


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