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Supplemental Oxygen Study

NCT02464917 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2019-08-22

Study results available
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Summary

The purpose of this study is to compare umbilical cord gases in subjects receiving oxygen at 10L/min via simple facemask to subjects receiving room air in those presenting for scheduled cesarean sections.

Conditions

  • Cesarean Section
  • Supplemental Oxygen
  • Umbilical Cord Gases

Interventions

DEVICE

Device: simple facemask to administer supplemental oxygen

Sponsors & Collaborators

  • MemorialCare Health System

    lead OTHER

Principal Investigators

  • Michael Nageotte, MD · MemorialCare Health System

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2015-10-31
Completion
2015-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02464917 on ClinicalTrials.gov