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NCT01047098 · ClinicalTrials.gov registry record · NA
Effects of Taking Prenatal Vitamin-mineral Supplements During Lactation on Iron Status and Markers of Oxidation
A NA study of Oxidative Stress and Iron Deficiency Anemia, sponsored by University of California, Davis.
- Completed
- Registry status
- NA
- Development phase
- 114
- Enrollment target
- 1
- Study location
NCT01047098 is a NA study of Oxidative Stress and Iron Deficiency Anemia that has completed, run by University of California, Davis. The registered enrollment target is 114 participants, above the 83-participant average among 36 other Oxidative Stress trials with a reported enrollment target (37% higher). The trial reports 1 study location across 1 state.
The verdict
NCT01047098, a NA study of Oxidative Stress and Iron Deficiency Anemia, has completed, sponsored by University of California, Davis.
- COMPLETED
- Registry status
- NA
- Development phase
- 114 participants
- Enrollment target
- 1
- Study location
Study Summary
Most breastfeeding women are told by their health care provider to continue taking prenatal vitamins after they give birth. A woman's requirement for iron while breastfeeding is low, yet prenatal vitamins contain a large amount of iron. The purpose of this study is to see if breastfeeding women are getting too much iron when taking prenatal vitamins.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Iron
Study Locations (1)
California
- UC Davis Medical Center - Sacramento
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 114 participants |
| Start Date | 2008-10 |
| Est. Completion | 2010-04 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01047098
The ClinicalTrials.gov registry entry for NCT01047098 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 114 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 83-participant average among 36 other Oxidative Stress trials with a reported enrollment target (37% higher). The listed sponsor is University of California, Davis, which has 657 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Oxidative Stress appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT01047098 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT01047098 about?
NCT01047098 is a clinical study titled "Effects of Taking Prenatal Vitamin-mineral Supplements During Lactation on Iron Status and Markers of Oxidation". Most breastfeeding women are told by their health care provider to continue taking prenatal vitamins after they give birth. A woman's requirement for iron while breastfeeding is low, yet prenatal vitamins contain a large amount of iron. The purpose of this study is to see if breastfeeding women are ...
What is the current status of trial NCT01047098?
This trial is currently completed. It is a NA study. The enrollment target is 114 participants. The study started on 2008-10. Estimated completion is 2010-04.
What conditions does trial NCT01047098 study?
This clinical trial studies the following conditions: Oxidative Stress, Iron Deficiency Anemia, Iron Overload.
What interventions are being tested in trial NCT01047098?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Iron (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT01047098?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01047098 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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