CompletedNot Applicable

Reference Ranges for Placental Perfusion Using Magnetic Resonance Imaging (MRI)PLACENTIMAGE

France135 participantsStarted 2010-02

Plain-language summary

To evaluate the feasibility of functional MRI method developed in an animal model and to construct normal reference ranges for in vivo placental perfusion using functional MRI. This will be based on imaging studies in patients undergoing termination of pregnancy (TOP) at 16 to 32 weeks' for fetal reason in a tertiary referral center.

Who can participate

Age range18 Years

SexFEMALE

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

Inclusion Criteria: * Women \> 18 years, * Undergoing TOP for fetal reason, * Informed signed consent. Exclusion Criteria: * Placental adhesion anomaly, * Growth restriction, * Contrast agent allergy, * Absent consent, * Contraindication of MRI or Gadolinium, * Renal insufficiency, * Placental abnormality at pathological examination.

What they're measuring

Establishment of physiological reference range of placental perfusion

Timeframe: 45 MIN

Trial details

NCT IDNCT01092949

SponsorAssistance Publique - Hôpitaux de Paris

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2018-03

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