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Construction of a Full-chain preterm birth prediction and prevention system based on maternal cohort

Construction of a Full-chain preterm birth prediction and prevention system based on maternal cohort

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066895
Enrollment
Unknown
Registered
2022-12-21
Start date
2022-12-30
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cervical incompetence

Interventions

Cerclage group:cervical cerclage
control group:Vaginal progesterone
sample colection:No.

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Cohort study. ? All pregnant women who attended our hospital during the study period and had their delivery cards established. ? Voluntary participation in this study and signing of informed consent form. 2. RCT study. ? Singleton pregnancies between 24 and 28 weeks of gestation. (ii) History of one or two previous midtrimester miscarriages or preterm deliveries at 16-34 weeks of gestation. (iii) cervical length =25 mm on transvaginal ultrasound. ? Voluntary participation in this study and signing of the informed consent form. Note: The study was included if both of the above conditions were met 3. To explore the predictive value of PYGL in cervical mucus for CI. ? All pregnant women who attended our hospital during the study period and had their delivery cards established. ? Voluntary participation in this study and signing of the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Cohort study. ? High sequence multiple pregnancies. ? with mental illness or cognitive impairment. 2. RCT studies. ? Those with painless cervical dilatation. ? active contractions. ? chorioamnionitis. ? abnormal antepartum hemorrhage. ? premature rupture of membranes. (6) Fatal fetal malformation or stillbirth. (7) Severe obstetric complications or comorbidities. ? Cervical cerclage or placement of a cervical support has been performed before or during pregnancy. Note: Subjects who meet any of the above criteria should be excluded. 3. To explore the predictive value of PYGL in cervical mucus for CI. ? High sequence of multiple pregnancies. ? Suffering from mental illness or cognitive impairment.

Design outcomes

Primary

MeasureTime frame
Diagnosis until the gestational interval;

Secondary

MeasureTime frame
Gestational age of delivery;perinatal mortality rate;neonate birth weight;postpartum hemorrhage;laceration of cervix;

Countries

China

Contacts

Public ContactMing Liu

Shanghai East Hospital (East Hospital Affiliated to Tongji University)

liuming7678@163.com13371985045

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026