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NCT03523455 · ClinicalTrials.gov registry record · NA
Iron Aid IPS on Performance, Fatigue and Iron Levels During 12 Weeks of Supplementation and Aerobic Training
A NA study, sponsored by University of Mary Hardin-Baylor.
- Terminated
- Registry status
- NA
- Development phase
- 2
- Enrollment target
NCT03523455 is a NA study that was terminated before completion, run by University of Mary Hardin-Baylor. The registered enrollment target is 2 participants.
The verdict
NCT03523455, a NA study, was terminated before completion, sponsored by University of Mary Hardin-Baylor.
- TERMINATED
- Registry status
- NA
- Development phase
- 2 participants
- Enrollment target
Study Summary
Participants are required to undergo a screening and qualification before beginning the study. Once qualified, baseline testing is completed in the laboratory. This testing includes: body composition measurements, a blood draw, questionnaires, a VO2 max test, and a time to exhaustion trial. This testing is repeated during week 4 and week 12. At week 8, subjects complete a blood draw and questionnaires only. During the 12 week period, participants will follow an endurance exercise program in which they will train 4 days per week. This is a double-blind study in which participants are randomized into either the placebo or supplement group. They are instructed to ingest the supplement once a day at breakfast. Diet logs are also monitored throughout the duration of the study with the restriction of no red meat.
Interventions
- OTHER Sugar Pill
- DIETARY_SUPPLEMENT Iron Aid IPS (Iron Protein Succinylate)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2 participants |
| Start Date | 2016-11-29 |
| Est. Completion | 2017-11-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03523455
The ClinicalTrials.gov registry entry for NCT03523455 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 2 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Mary Hardin-Baylor, which has 10 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Sugar Pill is the first listed.
NCT03523455 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03523455 about?
NCT03523455 is a clinical study titled "Iron Aid IPS on Performance, Fatigue and Iron Levels During 12 Weeks of Supplementation and Aerobic Training". Participants are required to undergo a screening and qualification before beginning the study. Once qualified, baseline testing is completed in the laboratory. This testing includes: body composition measurements, a blood draw, questionnaires, a VO2 max test, and a time to exhaustion trial. This tes...
What is the current status of trial NCT03523455?
This trial is currently terminated. It is a NA study. The enrollment target is 2 participants. The study started on 2016-11-29. Estimated completion is 2017-11-11.
What interventions are being tested in trial NCT03523455?
The interventions under investigation include: Sugar Pill (OTHER), Iron Aid IPS (Iron Protein Succinylate) (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT03523455?
This trial is sponsored by University of Mary Hardin-Baylor, which has 10 total clinical trials registered on ClinicalTrials.gov.
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