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RECRUITING Phase 4

Iron Deficiency Anemia (IDA) and the Brain

NCT05929729 · View on ClinicalTrials.gov ↗

Study Summary

This is a trial with an observational and an interventional arm, in patients with moderate to severe anemia and control subjects. The main purposes of this study is to phenotype the scope of neurocognitive deficits from iron deficiency anemia (IDA) in adult women, determine derangements in cerebral perfusion, vascular reactivity, functional connectivity, and blood brain barrier permeability in adult-onset IDA and relate them to neurocognitive deficits, as well as determine the reversibility and durability of both the physiologic and neurocognitive derangements by iron replacement therapy. All eligible subjects will be asked to provide informed consent before participating in the study.

Interventions

  • DRUG Ferric derisomaltose
  • DRUG NovaFerrum

Study Locations (4)

California

  • City of Hope Blood Donor Center — Duarte
  • Cedar Sinai Blood Bank — Los Angeles
  • Children's Hospital Los Angeles — Los Angeles
  • University of California, Los Angeles Blood Donor Center — Los Angeles

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2023-12-07
Est. Completion 2028-09-01
Phase Phase 4

Sponsor

Children's Hospital Los Angeles

163 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05929729

The ClinicalTrials.gov registry entry for NCT05929729 describes a study currently listed as recruiting. It is categorized as Phase 4, 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 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Hospital Los Angeles, which has 163 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Anemia appearing as the primary indexed condition, and to 2 interventions — of which Ferric derisomaltose 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: NCT05929729 reports 4 study locations spanning 1 distinct geographic area — top geographies include California. 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 NCT05929729 about?

NCT05929729 is a clinical study titled "Iron Deficiency Anemia (IDA) and the Brain". This is a trial with an observational and an interventional arm, in patients with moderate to severe anemia and control subjects. The main purposes of this study is to phenotype the scope of neurocognitive deficits from iron deficiency anemia (IDA) in adult women, determine derangements in cerebral ...

What is the current status of trial NCT05929729?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2023-12-07. Estimated completion is 2028-09-01.

What conditions does trial NCT05929729 study?

This clinical trial studies the following conditions: Anemia, Iron Deficiency Anemia, Anemia, Iron Deficiency, IDA - Iron Deficiency Anemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05929729?

The interventions under investigation include: Ferric derisomaltose (DRUG), NovaFerrum (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05929729?

This trial is sponsored by Children's Hospital Los Angeles, which has 163 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05929729 being conducted?

This trial has 4 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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