New ultrasound technique could unlock secrets of placental health in pregnancy
NCT ID NCT06497959
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study uses a special contrast dye (SonoVue) during ultrasound to look at blood flow in the placenta of pregnant women with fetal growth restriction. The goal is to better understand how the placenta works when the baby is not growing well. Thirty women who have already decided to end their pregnancy for medical reasons will take part, and the results may help doctors learn more about placental problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SonoVue (contrast agent for ultrasound)
- What this could lead to
- If successful, this could lead to better understanding of placental blood flow problems in fetal growth restriction, potentially guiding future treatments.
- What could go wrong
- This is a small, early-phase study (30 participants) focused on understanding, not treatment. The contrast agent's safety in pregnancy is still being studied, and results may not apply to all cases.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Apr 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 64 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult woman (age ≥18 years), * Gestational age between 16 GW + 0 days and 38 GW + 6 days, * Singleton pregnancy, * Whose request of a medical termination of pregnancy (IMG) has been formulated and accepted in a written form by the Centre Pluridisciplinaire de Diagnostic Prénatal (CPDPN) of the Centre Hospitalier Régional Universaitaire (CHRU) de Nancy, * Affiliated to the social security system or benefit from such a system, * Having received full information and having signed an informed consent form. Criteria specific to patients in the "growth restriction" group: \- Severe growth restriction defined by an estimation of foetal weight below the 3rd percentile using ultrasound performed no more than 15 days prior to the IMG (the diagnosis must be established at the time of the request for IMG in routine care). Exclusion Criteria: * Person who do not speak French * Any medical condition contraindicating the administration of SonoVue, in particular: * Hypersensitivity to sulfur hexafluoride or to one of the other components of SonoVue® such as polyethylene glycol (PEG), * Women with recent acute coronary syndrome or unstable ischaemic heart disease, * Women with a right-to-left shunt, severe pulmonary arterial hypertension (pulmonary arterial pressure \> 90 mmHg), uncontrolled systemic hypertension and women suffering from respiratory distress syndrome. * Persons covered by articles L. 1121-5, L. 1121-7 and L1121-8 of the French Public Health Code: * Breast-feeding mother * Minor (not emancipated) * An adult subject to a legal protection (guardianship, curatorship, safeguard of justice) * An adult unable to give consent * Persons deprived of their liberty by a judicial or administrative decision, persons under psychiatric care by virtue of articles L. 3212-1 and L. 3213-1
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CHRU de NANCY
RECRUITINGNancy, 54000, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Fetal heart strain: a new way to catch growth problems in twins?
- Can a simple ultrasound spot hidden heart strain in Growth-Restricted pregnancies?
- Can fetal heart scans predict risk in growth restriction?
- Ultrasound may predict hidden placental problems before delivery
- Placental protein clues may unlock mystery of poor fetal growth
- New doppler study aims to spot fetal distress earlier in Growth-Restricted pregnancies