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NCT04363905 · ClinicalTrials.gov registry record · NA
Supplemental Iron Improves Submaximal Exercise Performance in Non-anemic Iron Depleted Women
A NA study, sponsored by Cornell University.
- Completed
- Registry status
- NA
- Development phase
- 68
- Enrollment target
NCT04363905 is a NA study that has completed, run by Cornell University. The registered enrollment target is 68 participants.
The verdict
NCT04363905, a NA study, has completed, sponsored by Cornell University.
- COMPLETED
- Registry status
- NA
- Development phase
- 68 participants
- Enrollment target
Study Summary
The specific aims of the current study were: 1) To determine the prevalence of IDNA in a sample of Mexican women of reproductive age and 2) To determine how iron supplementation in IDNA women influences physical work capacity during submaximal exercise . The researchers hypothesized that marginally iron depleted women will have improved physical work capacity during submaximal intermittent exercise tests after dietary iron supplementation. However, no improvement in peak maximal oxygen consumption after dietary iron supplementation because they will remain non-anemic.
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Ferrous sulfate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 68 participants |
| Start Date | 2000-04-01 |
| Est. Completion | 2000-12-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04363905
The ClinicalTrials.gov registry entry for NCT04363905 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 68 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cornell University, which has 66 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT04363905 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04363905 about?
NCT04363905 is a clinical study titled "Supplemental Iron Improves Submaximal Exercise Performance in Non-anemic Iron Depleted Women". The specific aims of the current study were: 1) To determine the prevalence of IDNA in a sample of Mexican women of reproductive age and 2) To determine how iron supplementation in IDNA women influences physical work capacity during submaximal exercise . The researchers hypothesized that marginally ...
What is the current status of trial NCT04363905?
This trial is currently completed. It is a NA study. The enrollment target is 68 participants. The study started on 2000-04-01. Estimated completion is 2000-12-31.
What interventions are being tested in trial NCT04363905?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Ferrous sulfate (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT04363905?
This trial is sponsored by Cornell University, which has 66 total clinical trials registered on ClinicalTrials.gov.
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