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NCT01042262 · ClinicalTrials.gov registry record · NA
Maternal Oxygen Use During Delivery and Cord Blood Superoxide Dismutase
A NA study of Oxidative Stress and Fetal Distress, sponsored by George Washington University.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT01042262 is a NA study of Oxidative Stress and Fetal Distress that has completed, run by George Washington University. The registered enrollment target is 60 participants, below the 84-participant average among 36 other Oxidative Stress trials with a reported enrollment target (29% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01042262, a NA study of Oxidative Stress and Fetal Distress, has completed, sponsored by George Washington University.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
When exposed to oxygen immediately after birth, newborns suffer from an oxidative stress with a significant decrease in serum concentration of the anti-oxidant enzyme superoxide dismutase. This oxidative stress has been consequently linked to the development of adverse outcomes in both premature and full term infants. In this study, we examined the effect of oxygen administration to delivering mothers immediately before and during labor on the newborn. In this randomized trial, we planned to measure superoxide dismutase in the umbilical cord blood when mothers received and did not receive oxygen..
Conditions Studied
Interventions
- OTHER Placebo
- OTHER Oxygen
Study Locations (1)
District of Columbia
- The George Washington University Hospital - Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2007-02 |
| Est. Completion | 2009-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01042262
The ClinicalTrials.gov registry entry for NCT01042262 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 84-participant average among 36 other Oxidative Stress trials with a reported enrollment target (29% lower). The listed sponsor is George Washington University, which has 133 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Oxidative Stress appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT01042262 reports 1 study location spanning 1 distinct geographic area - top geographies include District of Columbia.
Frequently Asked Questions
What is clinical trial NCT01042262 about?
NCT01042262 is a clinical study titled "Maternal Oxygen Use During Delivery and Cord Blood Superoxide Dismutase". When exposed to oxygen immediately after birth, newborns suffer from an oxidative stress with a significant decrease in serum concentration of the anti-oxidant enzyme superoxide dismutase. This oxidative stress has been consequently linked to the development of adverse outcomes in both premature and...
What is the current status of trial NCT01042262?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2007-02. Estimated completion is 2009-08.
What conditions does trial NCT01042262 study?
This clinical trial studies the following conditions: Oxidative Stress, Fetal Distress.
What interventions are being tested in trial NCT01042262?
The interventions under investigation include: Placebo (OTHER), Oxygen (OTHER).
Who is sponsoring clinical trial NCT01042262?
This trial is sponsored by George Washington University, which has 133 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01042262 being conducted?
This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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