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Continuous Fetal Monitoring During Vacuum Delivery

NCT00956826 · Status: UNKNOWN · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2009-08-11

No results posted yet for this study

Summary

The investigators have added an additional electrode to the vacuum device for birth in which they can monitor the fetus during delivery.

Conditions

  • Vacuum Delivery

Interventions

DEVICE

Agit Vacuum

With an electrode and a regular vacuum device

Sponsors & Collaborators

  • Hadassah Medical Organization

    lead OTHER

Principal Investigators

  • David Mankuta, MD · Hadassah

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
1 Day
Max Age
1 Day
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2010-04-30
Completion
2010-12-31

Countries

  • Israel

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 NCT00956826 on ClinicalTrials.gov