RECRUITING

Oral Iron Supplementation on Alternate Vs. Consecutive Days for Iron Deficiency Anemia in Pregnancy

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This will be a randomized clinical trial. Enrolled subjects will be randomized (1:1) into two study arms to receive either daily (Group 1) or alternate day (Group 2) supplementation with one oral pill containing ferrous sulfate with an equivalent elemental iron dose of 65 mg per pill.

Official Title

Oral Iron Supplementation on Alternate Vs. Consecutive Days for Iron Deficiency Anemia in Pregnancy

Quick Facts

Study Start:2024-12
Study Completion:2028-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06492512

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 45 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Pregnant patients will be enrolled at less than 30 weeks gestational age (GA) with laboratory confirmed IDA (as defined by hemoglobin under 10.5 g/dL, as well as ferritin under 15 mcg/L)
  1. * Patients \<18 years old, patients who have severe IDA that requires blood transfusion or IV iron infusion, patients who have other known hemoglobinopathy (such as thalassemia or sickle cell anemia) or anemia of different mechanism (such as vitamin B12 or folate deficiency), patients with ulcerative colitis, Crohn's disease, gastric ulcers, patients who have previously undergone gastric bypass surgery, patients who experience admission for antepartum bleed, have been diagnosed with abnormal placentation (i.e., placenta previa, placenta accreta, placenta increta or percreta)

Contacts and Locations

Study Contact

Kathleen A Groesch, MS
CONTACT
217-545-6671
kgroesch@siumed.edu
Teresa S Wilson, BA
CONTACT
217-545-6711
twilson2@siumed.edu

Principal Investigator

Yahia Zeino, MD
PRINCIPAL_INVESTIGATOR
Southern Illinois University School of Medicine

Study Locations (Sites)

Southern Illinois University School of Medicine
Springfield, Illinois, 62702
United States

Collaborators and Investigators

Sponsor: Southern Illinois University

  • Yahia Zeino, MD, PRINCIPAL_INVESTIGATOR, Southern Illinois University School of Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12
Study Completion Date2028-06-30

Study Record Updates

Study Start Date2024-12
Study Completion Date2028-06-30

Terms related to this study

Keywords Provided by Researchers

  • Iron-deficiency anemia (IDA)
  • Iron-deficiency anemia (IDA) during gestation

Additional Relevant MeSH Terms

  • Iron-deficiency Anemia (IDA)
  • Pregnancy