Clinical trial

Peking University Birth Cohort in Weifang (PKUBC-WF)

Recruiting now · Not applicable · 1 countries · Registry ID NCT06234332

Recruiting nowNot applicableObservational

What this study is about

The PKUBC-WF is a prospective cohort study carried out in Weifang city of Shandong, China. The primary aim of this study is to investigate the short-term and long-term effects of pre-pregnant and prenatal exposure on maternal and child health. Data are collected regarding environmental, nutritional and lifestyle exposures as well as short-term and long-term health outcomes of mothers and their children from birth to before 18 years old. Biological samples including peripheral blood, urine, placenta, umbilical cord, cord blood, and faeces are also collected.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to Not listed

SexAll

Healthy volunteersAccepted

ConditionHealth Problems in Pregnancy, Pregnancy Outcomes, Gestational Diabetes, Gestational Hypertension, Preterm Birth, Obesity, Mother-Infant Interaction, Child Development, Anemia

Full registry criteria

Inclusion Criteria: * Pregnant woman 1. Pregnant women, 6-13\^+6 gestational weeks 2. Resided in Weifang in the past half years and have no plan to move out after delivery 3. Pregnant women who plan to have antenatal care and delivery in Weifang maternal\&Child Hospital. 4. Pregnant women who is willing to participate in this study with informed consent * Pregnant woman's husband 1. His wife was eligible for enrollment 2. He is the biological father of the child (his wife's current pregnancy) 3. Pregnant women's husband who is willing to participate in this study with informed consent * Offspring 4. Children born to pregnant women who met the inclusion criteria after enrolling in this study. 5\. Before the age of 8 years, his/her mother provided written informed consent. 6. After 8 years old, he/she agreed to continue this study and signed the informed consent. Exclusion Criteria: * Participants who cannot communicate normally.

Treatments and study arms

No Interventions

Other

No intervention This is an observational study without any intervention

Primary outcomes

Numbers and morbidity of participants with pregnancy complicationsAt delivery

Including gestational diabetes, gestational hypertension, anemia, and hypothyroidism during pregnancy

Numbers and morbidity of participants with adverse pregnancy outcomesAt delivery

Including preterm birth, low birth weight, macrosomia, abortion, stillbirth, and birth defects.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Peking University🇨🇳 Beijing, Beijing Municipality, China

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Haijun Wang, Ph.DContact

Email · Call 86-010-82805583

Jue Liu, Ph.DContact

Email · Call 86-13426455743