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NCT06232642 · ClinicalTrials.gov registry record · NA
Effects of Lactoferrin-enriched Whey on Iron Status in Females
A NA study of Serum Ferritin, sponsored by Utah State University.
- Active
- Registry status
- NA
- Development phase
- 82
- Enrollment target
- 1
- Study location
NCT06232642 is a NA study of Serum Ferritin that is active but no longer recruiting, run by Utah State University. The registered enrollment target is 82 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06232642, a NA study of Serum Ferritin, is active but no longer recruiting, sponsored by Utah State University.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 82 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this work is to study the effects of twice daily ingestion of a whey protein, rice protein, or maltodextrin drink enriched with lactoferrin- (200 mg), iron (6 mg) and vitamin B12 (5.2 µg) for 16-weeks on iron metabolism and inflammatory markers in active young females. It is expected that the females consuming containing lactoferrin-, iron, and vitamin B12-enriched whey will 1) improve serum ferritin status; 2) reduce inflammation; 3) improve markers of iron metabolism, such as Hemoglobin (Hb), red blood cell count (RBC) and hematocrit (Hc) compared to women who consume the rice protein or maltodextrin control drink. Blood will be drawn before the beginning of the supplemental period (week 0) and end the end of the intervention phase (week 16).
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Lactoferrin, iron and B12 in Whey Protein
- DIETARY_SUPPLEMENT Lactoferrin, Iron and B12 in Rice Protein
- DIETARY_SUPPLEMENT Lactoferrin, Iron and B12 in Maltrodextrin
Study Locations (1)
Utah
- Center for Human Nutrition Studies - Logan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 82 participants |
| Start Date | 2024-03-01 |
| Est. Completion | 2025-05-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06232642
The ClinicalTrials.gov registry entry for NCT06232642 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 82 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Utah State University, which has 27 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Serum Ferritin appearing as the primary indexed condition, and to 3 interventions - of which Lactoferrin, iron and B12 in Whey Protein is the first listed.
NCT06232642 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.
Frequently Asked Questions
What is clinical trial NCT06232642 about?
NCT06232642 is a clinical study titled "Effects of Lactoferrin-enriched Whey on Iron Status in Females". The goal of this work is to study the effects of twice daily ingestion of a whey protein, rice protein, or maltodextrin drink enriched with lactoferrin- (200 mg), iron (6 mg) and vitamin B12 (5.2 µg) for 16-weeks on iron metabolism and inflammatory markers in active young females. It is expected tha...
What is the current status of trial NCT06232642?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 82 participants. The study started on 2024-03-01. Estimated completion is 2025-05-30.
What conditions does trial NCT06232642 study?
This clinical trial studies the following conditions: Serum Ferritin.
What interventions are being tested in trial NCT06232642?
The interventions under investigation include: Lactoferrin, iron and B12 in Whey Protein (DIETARY_SUPPLEMENT), Lactoferrin, Iron and B12 in Rice Protein (DIETARY_SUPPLEMENT), Lactoferrin, Iron and B12 in Maltrodextrin (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT06232642?
This trial is sponsored by Utah State University, which has 27 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06232642 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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