UnknownNot Applicable

Prediction of Late Fetal Growth Restriction Using Cerebroplacental Ratio

Egypt200 participantsStarted 2021-02-01

Plain-language summary

To investigate the screening performance of CPR and biophysical profile score for the prediction of composite of adverse neonatal morbidity and mortality and operative delivery (CS or instrumental) for intrapartum fetal distress in low-risk pregnancies

Who can participate

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * •Women with uncomplicated singleton pregnancy who are planning a vaginal delivery * Gestational age from 36 ± 0/7 weeks until onset of active labor (cervical dilatation ≤ 4cm) * Cephalic presentation Exclusion Criteria: * •Multiple pregnancy * known SGA fetus. * Medical disorders with pregnancy: diabetes mellitus, hypertension, pre-eclampsia * Known fetal anomaly or aneuploidy or stillbirth. * Any contraindication of vaginal delivery eg. placenta previa.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

A composite of adverse neonatal outcomes

Timeframe: Up to 48 hours After delivery

Trial details

NCT IDNCT04640467

SponsorAssiut University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2022-10-01

Contact for this trial

Mariam Sobhy, MBBCH

+201095811120 rrrrgds83@gmail.com

View on ClinicalTrials.gov More Fetal Growth Retardation trials

Who can participate

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.