Treatment of Non-Anemic Iron Deficiency in Pregnancy
Public ClinicalTrials.gov record NCT05423249. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Treatment of Non-Anemic Iron Deficiency in Pregnancy: a Double-Blind Randomized Control Trial
Study identification
- NCT ID
- NCT05423249
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Not applicable
- Lead sponsor
- Stony Brook University
- Other
- Enrollment
- 150 participants
Conditions and interventions
Conditions
Interventions
- Ferrous sulfate Drug
- Prenatal Drug
- Docusate Sodium Drug
- Ascorbic Acid 500Mg Tab Drug
- Placebo Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years to 55 Years
- Sex
- Female
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 11, 2022
- Primary completion
- Oct 31, 2024
- Completion
- Nov 14, 2024
- Last update posted
- Nov 28, 2024
2022 – 2024
United States locations
- U.S. sites
- 3
- U.S. states
- 1
- U.S. cities
- 3
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University Associates in Obstetrics & Gynecology | Bohemia | New York | 11716 | — |
| University Associates in Obstetrics & Gynecology | Commack | New York | 11725 | — |
| University Associates in Obstetrics & Gynecology | East Setauket | New York | 11733 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT05423249, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Nov 28, 2024 · Synced Jul 22, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT05423249 live on ClinicalTrials.gov.