CompletedNot Applicable

Value of Measuring Cervical Angle and Length by Ultrasound in Prediction of Successful Induction of Delivery

Egypt70 participantsStarted 2017-04-15

Plain-language summary

Seventy ladies indicated for induction of delivery will be recruited. Two ways of assessment of their cervices will be done before actual induction of labor. First, ultrasound will be done to assess the angle and the length of the cervix. Then vaginal examination will be done to assess the characteristics of cervix. Analysis will be done to identify the best predictor of successful induction of labour.

Who can participate

Age range

18 Years – 37 Years

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: * Singleton pregnancy * Gestational age between 35 and 42 * Presence of an indication for induction of labour as post-term pregnancy or rupture of membranes * The fetus is living * Cephalic presentation Exclusion Criteria: * Estimated fetal weight more than 4 kilograms * Malpresentation * Oligohydramnios * Polyhydramnios * Non-reassuring non-stress test before induction of labor * Cephalo-pelvic disproportion * Previous operation on the cervix as cautery or cerclage * Previous cesarean section * Any contraindication to vaginal delivery including placenta previa * Anomalous fetus * Morbid obesity

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

Value of posterior cervical angle

Timeframe: At around 10 minutes from admission to hospital

Trial details

NCT IDNCT03113227

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-07-09

View on ClinicalTrials.gov More Induced; Birth trials