Performance Evaluation of System EOS Imaging in Pelvimetry Versus Pelvi-scanner

NCT ID: NCT02834897

Last Updated: 2018-07-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-05-31

Study Completion Date

2016-02-12

Brief Summary

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The purpose of this study and demonstrate the reliability of EOS imaging system in the measurement of internal diameters of obstetrical pelvis versus "Goldstandard current "that is the pelviscanner.

Detailed Description

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Conditions

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Radiation Obstetric Labor Complications Pregnancy Complications

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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EOS and CT Exam

EOS and CT Examen for pregnant women in the 8th month of pregnancy

Group Type EXPERIMENTAL

EOS and CT Exam

Intervention Type RADIATION

EOS and CT Examen for pregnant women in the 8th month of pregnancy

Interventions

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EOS and CT Exam

EOS and CT Examen for pregnant women in the 8th month of pregnancy

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* pelviscanner indication in women

Exclusion Criteria

* In the disqualification of another study or under the "national register of volunteers."
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Besancon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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sebastien AUBRY, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Besancon

Locations

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CHRU de Besançon

Besançon, , France

Site Status

Countries

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France

Other Identifiers

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P/2014/236

Identifier Type: -

Identifier Source: org_study_id

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