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Recruiting NCT06314009

NCT06314009 Beyond MARS: Magnetic Resonance Study: A Novel Assessment of Placental Perfusion During Pregnancy

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Clinical Trial Summary
NCT ID NCT06314009
Status Recruiting
Phase
Sponsor Endeavor Health
Condition Pregnancy
Study Type OBSERVATIONAL
Enrollment 30 participants
Start Date 2024-05-09
Primary Completion 2026-12

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 60 Years
Study Type OBSERVATIONAL
Interventions
functional Magnetic Resonance Imaging (fMRI)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 30 participants in total. It began in 2024-05-09 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to evaluate the flow of oxygen and blood necessary for nutrient transfer across the placenta during the second and third trimesters in pregnancy in women who are obese before pregnancy compared to women who have an average weight before pregnancy. This study will evaluate blood flow across the placenta by functional Magnetic Resonance Imaging (fMRI). The investigators hypothesize that there will be differences in placental oxygenation and blood flow among women with obesity as compared to those with normal weight. Participants will be asked to complete: * MRI in the second trimester (20-24 weeks) * MRI in the third trimester (30-34 weeks)

Eligibility Criteria

Inclusion Criteria: * Singleton pregnancy, less than 24 weeks gestation * Pre-pregnancy BMI between 18.5 - 24.9kg/m2 or ≥30kg/m2 Exclusion Criteria: * Asthma on controller medication * Autoimmune Conditions * Chronic Hypertension * Claustrophobia * Congenital Anomaly * Pregestational Diabetes * History of Bariatric Surgery * HIV * Ineligible for MRI (incompatible implanted medical device) * Multifetal Gestation * Smoking during pregnancy

Contact & Investigator

Central Contact

Alexandra Mangus

✉ alexandra.mangus@endeavorhealth.org

📞 (847) 570-2243

Principal Investigator

Caitlin MacGregor

PRINCIPAL INVESTIGATOR

Endeavor Health

Frequently Asked Questions

Who can join the NCT06314009 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 60 Years, studying Pregnancy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06314009 currently recruiting?

Yes, NCT06314009 is actively recruiting participants. Contact the research team at alexandra.mangus@endeavorhealth.org for enrollment information.

Where is the NCT06314009 trial being conducted?

This trial is being conducted at Evanston, United States.

Who is sponsoring the NCT06314009 clinical trial?

NCT06314009 is sponsored by Endeavor Health. The principal investigator is Caitlin MacGregor at Endeavor Health. The trial plans to enroll 30 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology