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| ID | Type | Description | Link |
|---|---|---|---|
| R01EB017337-01 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| Massachusetts General Hospital | OTHER |
| Massachusetts Institute of Technology | OTHER |
| National Institute for Biomedical Imaging and Bioengineering (NIBIB) | NIH |
The ultimate goal of this project is to develop methods that allow informed decision-making on the delivery time of fetuses that are at increased risk of stillbirth due to IUGR. In placenta related IUGR pregnancies, there can be multiple concurrent placental pathologies. Although there is no specific correspondence between a single type of pathology and IUGR, the common result of these pathologies is placental insufficiency, which limits the maternal-fetal exchange. Oxygen and nutrition transport is known to be hindered in IUGR placentas due to obstructed or abrupt vasculature, massive fibrin deposition, and inflammation in the villous and intervillous space (villitis). Thus one potential approach to distinguish IUGR pregnancies from normal ones is to assess the efficiency of placental transport. Based on the hypothesis that efficiency of oxygen transport is representative for overall oxygen and nutrition transport in placenta, the investigators propose to characterize the blood oxygenation and blood perfusion in placenta in vivo via MRI, and use it as an index for better stratification in the IUGR risk group. The investigators will also consider alternative MRI approaches such as structural, diffusion and spectroscopy measurements inside the placenta, which might reflect the state of placental transport and reveal the status of placental health.
Specific aims: 1) To correlate the MRI metrics that differentiate placental insufficiency from normal placenta transport with histopathology data of the placenta. 2) To correlate the MRI metrics that reflects placental insufficiency with fetal outcome
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| all subjects | For all subjects, administration of oxygen will last for no more than 10 min, with flow rate 15L/min via non-rebreather facial mask. Each subject will have once of the administration per scan. Data collection will start about 10 min before the administration of oxygen, and last throughout the oxygen exposure, then continue for about 10 min after oxygen exposure for each subject. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Oxygen | Other | Administration of oxygen will last for no more than 10 min, with flow rate 15L/min via non-rebreather facial mask. Each subject will have once of the administration per scan. |
| Measure | Description | Time Frame |
|---|---|---|
| BOLD MRI signal change during maternal oxygen exposure in placenta and fetus | 30 min during the 1 hour scan | |
| placental volume on MRI image | 5 min during 1 hour scan |
| Measure | Description | Time Frame |
|---|---|---|
| pathological reports of placenta after delivery | 1 day | |
| fetal growth curve after birth | up to 6 month |
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Inclusion Criteria:
The pregnant mother with twin gestation with diagnosis of selective IUGR based upon obstetrical US findings as following:
The pregnant mother with singleton gestation with diagnosis of IUGR based upon obstetrical US findings as following:
Gestational age: Bigger than 18 weeks.
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.
Pregnant mothers with the following features will be excluded.
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| Name | Affiliation | Role |
|---|---|---|
| Patricia E Grant, MD | Boston Children's Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Boston Children's Hospital | Recruiting | Boston | Massachusetts | 02115 | United States |
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| ID | Term |
|---|---|
| D005317 | Fetal Growth Retardation |
| ID | Term |
|---|---|
| D005315 | Fetal Diseases |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
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| ID | Term |
|---|---|
| D010100 | Oxygen |
| ID | Term |
|---|---|
| D018011 | Chalcogens |
| D004602 | Elements |
| D007287 | Inorganic Chemicals |
| D005740 | Gases |
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| Madrid-MIT M+Visión Consortium |
| UNKNOWN |
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| Hospital Universitario de Fuenlabrada | Recruiting | Madrid | 28942 | Spain |
|
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D006130 | Growth Disorders |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |