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NCT02038023 · ClinicalTrials.gov registry record · Phase 2
Intravaneous Iron(1000 mg Low Molecular Weight Iron Dextran Over 60 Minutes) for Pregnant Women
A Phase 2 study of Pregnancy, sponsored by Auerbach Hematology Oncology Associates P C.
- Completed
- Registry status
- Phase 2
- Development phase
- 74
- Enrollment target
- 1
- Study location
NCT02038023 is a Phase 2 study of Pregnancy that has completed, run by Auerbach Hematology Oncology Associates P C. The registered enrollment target is 74 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02038023, a Phase 2 study of Pregnancy, has completed, sponsored by Auerbach Hematology Oncology Associates P C.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 74 participants
- Enrollment target
- 1
- Study location
Study Summary
To determine the percentage of women who achieve anemia correction after a single dose of 1000mg of low molecular weight iron dextran(infed).
Conditions Studied
Interventions
- DRUG Intravaneous iron(low molecular weight iron dextran)
Study Locations (1)
Maryland
- Auerbach Hematology Oncology Assoc - Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2013-07 |
| Est. Completion | 2015-08 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02038023
The ClinicalTrials.gov registry entry for NCT02038023 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 74 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (92% lower). The listed sponsor is Auerbach Hematology Oncology Associates P C, which has 5 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pregnancy appearing as the primary indexed condition, and to 1 intervention - of which Intravaneous iron(low molecular weight iron dextran) is the first listed.
NCT02038023 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT02038023 about?
NCT02038023 is a clinical study titled "Intravaneous Iron(1000 mg Low Molecular Weight Iron Dextran Over 60 Minutes) for Pregnant Women". To determine the percentage of women who achieve anemia correction after a single dose of 1000mg of low molecular weight iron dextran(infed).
What is the current status of trial NCT02038023?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 74 participants. The study started on 2013-07. Estimated completion is 2015-08.
What conditions does trial NCT02038023 study?
This clinical trial studies the following conditions: Pregnancy.
What interventions are being tested in trial NCT02038023?
The interventions under investigation include: Intravaneous iron(low molecular weight iron dextran) (DRUG).
Who is sponsoring clinical trial NCT02038023?
This trial is sponsored by Auerbach Hematology Oncology Associates P C, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02038023 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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