Gongji Pregnancy Endorine Cohort Study (NCT07125885) | Clinical Trial Compass
RecruitingNot Applicable
Gongji Pregnancy Endorine Cohort Study
China3,000 participantsStarted 2023-05-05
Plain-language summary
To explore the relationship between genetic factors, lifestyle, and drug interventions and the occurrence, development, adverse pregnancy outcomes, and postpartum maternal-infant outcomes of gestational endocrine diseases.
Who can participate
Age range
18 Years – 50 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:
* Women preparing for pregnancy or pregnant women or within 1 year after giving birth
* Age ≥ 18 years old
* Signed the informed consent form to voluntarily enroll in the management follow-up
Exclusion Criteria:
* Individuals who are unable to communicate normally and those who are unwilling to cooperate
* Pregnant women with severe organic diseases or mental illnesses
* Any condition deemed by the investigator to affect eligibility for the study
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
1
Composite adverse maternal and neonatal outcomes associated with gestational endocrine disorders
Timeframe: From delivery (Day 0) through the initial birth hospitalization, assessed up to 14 days postpartum.
2
Postpartum glucose metabolism outcomes in patients with endocrine disorders in pregnancy
Timeframe: From 6 weeks postpartum through long-term follow-up, with assessments at 6 weeks and every 12 months thereafter, for ≥3 years and up to 40 years postpartum.
3
Postpartum thyroid disease outcomes in patients with endocrine disorders in pregnancy
Timeframe: From 6 weeks postpartum through long-term follow-up, with assessments at 6 weeks and every 12 months thereafter, for ≥3 years and up to 40 years postpartum.