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NCT02834897 Clinical Trial

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

Pregnancy Complications Clinical Trial

— PELVI-EOS  

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02834897
Other study ID # P/2014/236
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2015
Est. completion date February 12, 2016

Study information
Verified date July 2016
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 36
Est. completion date February 12, 2016
Est. primary completion date February 12, 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- pelviscanner indication in women

Exclusion Criteria:

- In the disqualification of another study or under the "national register of volunteers."

Study Design

Related Conditions & MeSH terms

Intervention

Radiation:
• EOS and CT Exam
EOS and CT Examen for pregnant women in the 8th month of pregnancy

Locations
Country Name City State
France CHRU de Besançon Besancon

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measurement reliability index Magnin with EOS cab relative to the CT measurements one months
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