The Best Timing of Delivery in Women With GDM Study (NCT03928899) | Clinical Trial Compass
UnknownNot Applicable
The Best Timing of Delivery in Women With GDM Study
China230 participantsStarted 2019-07-15
Plain-language summary
The investigatiors aimed to conduct a well-designed RCT to firstly focus on GDM women controlled with only diet and exercise, and provide an optimize process on their timing and mode of delivery
Who can participate
Age range
18 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 pregnant women
* in vertex presentation
* GDM that is controlled with only diet and exercise
* at 37 weeks 0 days to 37 weeks 6 days of gestation
* more than 18 years old
* have no other contraindications to vaginal delivery.
Exclusion Criteria:
* prior caesarean section or myomectomy
* any known contraindications to vaginal delivery
* uncertain gestational age
* non reassuring foetal wellbeing necessitating delivery
* maternal pregnancy-related disease necessitating delivery (any hypertensive disorder, cardiac disease, renal insufficiency、immune diseases, et al.)
* placenta previa, accreta, vasa previa
* known foetal anomaly
* negative reproductive history
* ruptured membranes or known oligohydramnios (defined as AFI \< 5 or MVP \< 2 ) before 37weeks 6 days of gestation
* fetal growth restriction, defined as EFW \< 10th percentile
* known HIV positivity because of modified delivery plan
* signs of labor (regular painful contractions with cervical change) before 37weeks 6 days of gestation.
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.