EOS® Versus Spiral CT Technique for Achieving a Pelvimetry in Suites of Obstructed Labor: Comparative Single-center Prospective Study - PELVIC-EOS.
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 117
- Locations
- 1
- Primary Endpoint
- Diameter of the basin
Study Overview
Brief Summary
The aim of this study is to demonstrate in vivo the concordance of the imagery system EOS and the spiral CT in women having had an obstructed delivery. If this concordance is demonstrated, it would allow the use of this new technique of imagery, to realize a pelvimetry during the pregnancy less irradiating for the mother, and the fetus.
Detailed Description
The aim of this study is to demonstrate in vivo the concordance of the imagery system EOS and the spiral CT in women having had an obstructed delivery. If this concordance is demonstrated, it would allow the use of this new technique of imagery, to realize a pelvimetry during the pregnancy less irradiating for the mother, and the fetus.
To answer this objective, the study will be a prospective, monocentric, open clinical trial, comparing the radio-pelvimetry realized with EOS technique, to the spiral CT. Measures are performed in the 3 months following the obstructed delivery.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Diagnostic
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients who gave birth at the CHU Saint-Etienne
- •Patients having an indication of pelvimetry
- •Patients who delivered singleton pregnancy in cephalic presentation at term
- •Patients affiliated to a social security scheme
Exclusion Criteria
- •Patients with no wish of further pregnancy
- •Patients with another cause of dystocia during labor
- •Patients with a significant number (>2) of radiological examinations in the year before
Arms & Interventions
EOS + Spiral CT pelvimetry
Women with an indication of pelvimetry will be included in this study. They will be their own control because they will benefit from the two methods of diagnosis : EOS new technique, and spiral CT (usual technique).
Intervention: EOS (Device)
EOS + Spiral CT pelvimetry
Women with an indication of pelvimetry will be included in this study. They will be their own control because they will benefit from the two methods of diagnosis : EOS new technique, and spiral CT (usual technique).
Intervention: Spiral CT pelvimetry (Device)
Outcomes
Primary Outcomes
Diameter of the basin
Time Frame: Day 1
The aim of this study is to compare the measures of the basins with two different techniques : the usual one spiral CT technique, and the new one : the EOS technique that is less irradiating than the older one. If these two techniques give the same measures, researchers would be able in the future to use the new technique less invasive for the mother and the fetus, as a routine technique.
Secondary Outcomes
No secondary outcomes reported