MRI could help doctors decide when to deliver babies at risk of stillbirth
NCT ID NCT02297724
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study uses MRI scans to measure how well oxygen moves through the placenta in pregnancies complicated by intrauterine growth restriction (IUGR), where the baby is not growing as expected. Researchers will compare MRI results with placenta tissue after birth and track the baby's growth afterward. The goal is to develop a safe, non-invasive way to identify which babies are at highest risk and need early delivery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- oxygen
- What this could lead to
- If successful, this could lead to a non-invasive MRI test that helps doctors decide the safest time to deliver babies with growth problems, potentially reducing stillbirths.
- What could go wrong
- This is an early-stage observational study with only 80 participants. The MRI methods may not prove reliable enough for routine clinical use, and results may not apply to all types of IUGR.
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.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Apr 2014
- Expected to finish
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Sep 2028
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.
Who is studied
* pregnant mothers with twin gestation with diagnosis of selective IUGR * pregnant mothers with singleton gestation with diagnosis of IUGR * singleton pregnant mothers and twin pregnant mothers with no apparent medical complication on fetuses
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: 1. The pregnant mother with twin gestation with diagnosis of selective IUGR based upon obstetrical US findings as following: * Proven monochorionicity / dichorionicity * Discordance in estimated fetal weight (EFW). Growth restriction (\<10 percentile of norm) in one or both fetus(es) AND/OR growth discordance (\> or = 20%) between twin fetuses. 2. The pregnant mother with singleton gestation with diagnosis of IUGR based upon obstetrical US findings as following: * Proven singleton gestation * Growth restriction of fetus (\<10 percentile of norm) * Doppler measurements that indicates placental insufficiency: umbilical artery, middle cerebral artery, uterine artery; or oligohydramnios. 3. Gestational age: Bigger than 18 weeks. 4. Pregnant mother is between age 18 to 45, clinically stable and can safely tolerate fetal MRI study. Exclusion Criteria: Fetuses/infants with the following features will be excluded. 1. Fetus/infant with chromosomal anomalies or known genetic disorders. 2. Fetus/infant with other major congenital malformation. 3. Presence of any condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient, quality or completeness of the data. Pregnant mothers with the following features will be excluded. 1. Mothers with contraindication to MRI (with pacemaker, metal in body, oversize). 2. Mothers with claustrophobia 3. Mothers medically unstable for the MRI study
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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
2 sites in 2 countries. 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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Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
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Hospital Universitario de Fuenlabrada
RECRUITINGMadrid, 28942, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can early feeding shape a premature Baby's brain and body?
- Blood test may pinpoint cause of stunted fetal growth
- Scientists hunt for clues to pre-eclampsia in placenta and blood samples
- Can early speech therapy boost language in preterm babies?
- Blood thinner may help babies in womb with growth problems
- Ultrasound program aims to halve stillbirths by spotting tiny babies earlier.