CompletedNot Applicable

Comparison of Pelvimetric Measurements Between MRI and Low-dose Stereoradiography (EOS® Imaging System)

France35 participantsStarted 2021-11-09

Plain-language summary

The main objective of this study is to compare pelvimetric measurements performed by Magnetic Resonance Imaging (MRI) and by the EOS imaging system.

Who can participate

Age range

18 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients \> 18 years of age * Patient requiring pelvimetry (breech fetus) * Gestation \> 36 SA (weeks of amenorrhea) * Patients with BMI \< 35 * Affiliated to social security or similarly regime * Patients who gave their consent to participate in the study (Patient having agreed to perform both examinations: MRI and EOS system) Exclusion Criteria: * Patient with a contraindication to MRI (claustrophobia, pace-maker, intracorporeal metallic element) * Patient with a contraindication to performing EOS® (person not standing alone) * Patient who are in exlusion period of another interventiionnal study * Person deprived of freedom by judicial or administrative decision; person hospitalized for psychitric care; person under legal protection measure.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Estimation of the reliability of pelvimetric measurements using Transverse Inlet Diameter measurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using ante posterior diameter measurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using BiSpinous Diameter measurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using Bi-ischiatic mesurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using Magin's Index calculation

Timeframe: Up to 1 day

Trial details

NCT IDNCT04849975

SponsorUniversity Hospital, Grenoble

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-07-24

View on ClinicalTrials.gov More Breech Fetal Presentation trials

Who can participate

Age range

18 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Estimation of the reliability of pelvimetric measurements using Transverse Inlet Diameter measurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using ante posterior diameter measurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using BiSpinous Diameter measurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using Bi-ischiatic mesurement

Timeframe: Up to 1 day

Estimation of the reliability of pelvimetric measurements using Magin's Index calculation

Timeframe: Up to 1 day