RECRUITING

Pilot Trial Investigating Every Other Day Dosing of Oral Iron in Premature Infants (IQONic)

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

Study focuses on determining if daily versus every-other-day (EOD) oral iron at the same dose per kilogram per day will achieve similar incidence of iron replete status at 36 weeks post-menstrual age in premature neonates

Official Title

Pilot Non-inferiority Study Investigating Daily Versus Every Other Day Dosing of Oral Iron in Premature Infants.

Quick Facts

Study Start:2024-08-01
Study Completion:2026-03-28
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06555315

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:26 Weeks to 32 Weeks
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Children (Minor \< 18 years of age)
  2. * Neonates
  3. * Hospitalized
  4. * Premature infants who are on full enteral feeds and are started on oral iron
  5. * Premature infants who completed 26 0/7 to 32 6/7 weeks' gestation at birth
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Rosario Ocampo
CONTACT
210-704-4996
rosario.ocampo@christushealth.org
Donna Rodney
CONTACT
(210) 683-7746
donna.rodney@christushealth.org

Principal Investigator

Pratik K Parikh, MD
PRINCIPAL_INVESTIGATOR
CHRISTUS Health
Richelle L Homo, MD
PRINCIPAL_INVESTIGATOR
CHRISTUS Health; Brooke Army Medical Center

Study Locations (Sites)

CHRISTUS Children's
San Antonio, Texas, 78207
United States

Collaborators and Investigators

Sponsor: CHRISTUS Health

  • Pratik K Parikh, MD, PRINCIPAL_INVESTIGATOR, CHRISTUS Health
  • Richelle L Homo, MD, PRINCIPAL_INVESTIGATOR, CHRISTUS Health; Brooke Army Medical Center

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 Date2024-08-01
Study Completion Date2026-03-28

Study Record Updates

Study Start Date2024-08-01
Study Completion Date2026-03-28

Terms related to this study

Keywords Provided by Researchers

  • Premature infants
  • Iron
  • anemia of prematurity
  • iron deficiency

Additional Relevant MeSH Terms

  • Very Low Birth Weight Infant
  • Premature Infants
  • Anemia of Prematurity
  • Iron Deficiency, Anaemia in Children
  • Extremely Low Birth Weight