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Pilot Trial Investigating Every Other Day Dosing of Oral Iron in Premature Infants (IQONic)
NCT06555315 · View on ClinicalTrials.gov ↗
Study Summary
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
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT 6 mg/kg of oral iron as ferrous sulfate administered every other day.
- DIETARY_SUPPLEMENT 6 mg/kg of oral iron as ferrous sulfate administered every day.
Study Locations (1)
Texas
- CHRISTUS Children's — San Antonio
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-08-01 |
| Est. Completion | 2026-03-28 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06555315
The ClinicalTrials.gov registry entry for NCT06555315 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CHRISTUS Health, which has 31 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 5 conditions, with Premature Infants appearing as the primary indexed condition, and to 2 interventions — of which 6 mg/kg of oral iron as ferrous sulfate administered every other day. is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06555315 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06555315 about?
NCT06555315 is a clinical study titled "Pilot Trial Investigating Every Other Day Dosing of Oral Iron in Premature Infants (IQONic)". 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
What is the current status of trial NCT06555315?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-08-01. Estimated completion is 2026-03-28.
What conditions does trial NCT06555315 study?
This clinical trial studies the following conditions: Premature Infants, Very Low Birth Weight Infant, Anemia of Prematurity, Iron Deficiency, Anaemia in Children, Extremely Low Birth Weight. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06555315?
The interventions under investigation include: 6 mg/kg of oral iron as ferrous sulfate administered every other day. (DIETARY_SUPPLEMENT), 6 mg/kg of oral iron as ferrous sulfate administered every day. (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06555315?
This trial is sponsored by CHRISTUS Health, which has 31 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06555315 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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