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Fetal Pulse Oximetry Trial (FOX)

NCT00098709 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 10000

Last updated 2022-03-18

No results posted yet for this study

Summary

The purpose of this study is to determine if the information provided to the physician by a fetal pulse oximeter during labor will reduce the chances of a cesarean delivery.

Conditions

  • Pregnancy

Interventions

DEVICE

Fetal pulse oximeter

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH

  • The George Washington University Biostatistics Center

    lead OTHER

Principal Investigators

  • Cathy Spong, MD · Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

  • Elizabeth A Thom, Ph.D. · George Washington University Biostatistics Center

  • Steven L Bloom, M.D. · University of Texas

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2002-05-31
Completion
2005-02-28

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 NCT00098709 on ClinicalTrials.gov