Feasibility of performing Blood Oxygen Level-Dependent MRI of the placenta.

Completed

• Conditions: Placental function; placental oxygenation; 10035129

• Registration Number: NL-OMON48878
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 14

Inclusion Criteria

- Singleton, uncomplicated pregnancy between 28 and 34 weeks of gestation
- Understanding of Dutch in speaking and reading
- Signed informed consent (willingness to participate in the study)
- Minimal age of 18 years

Exclusion Criteria

- Unknown or uncertain gestational age
- Congenital anomalies detected by ultrasound
- Multiple pregnancy
- (Gestational) diabetes
- Preeclampsia or fetal growth restriction
- Claustrophobia (because of the necessity to be in an MRI chamber)
- Inability to give informed consent (e.g. mentally impaired)
- Women with a pacemaker, cochlear implants, neurostimulator or subcutaneous
insulin pump (contraindications for MRI).
- Not willing to be informed about incidental findings following the
performance of the MRI

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The percentage of participants with successful BOLD MRI.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable.</p><br>