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Miscarriage Preventing Herbal Medicines and the Risk of Birth Defects: a Population-based Cohort Study

S

Sichuan University

Status

Active, not recruiting

Conditions

Birth Defects
Drug Exposures
Pregnancy

Treatments

Drug: Herbal medicines (e.g., Yunkang granules, Duzhong granules)

Study type

Observational

Funder types

Other

Identifiers

NCT06048276
HERB and BD

Details and patient eligibility

About

Using data from a population-based medicine use cohort in Xiamen, China, this retrospective cohort study will investigate whether herbal medicines used to prevent miscarriage are associated with increased risk of birth defects.

Full description

Herbal medicines have a long history of use for pregnant women both in China and around the world. However, the safety of herbal medicines used at the early gestation is often questioned regarding their impact on offspring. Therefore, the aim of this study is to investigate whether miscarriage preventing herbal medicines associated with increased risk of birth defects.

A large medication use cohort will be developed by linking a population-based pregnancy registry (i.e., REPRESENT) and a population-based pharmacy database, which documented all prescriptions at both outpatients and inpatients from conception to delivery. This cohort will include herbal medicines formula which were granted approval by the Chinese National Medical Products Administration.

Using data from this cohort, the investigators will investigate the prevalence of the use of herbal medicine formulas and prescription patterns at the first trimester. This study will then investigate the association between miscarriage preventing herbal medicines and the risk of birth defects. A propensity score matching (PSM) based Poisson regression will be used to estimate the relative risk. To ensure the robustness of the results investigators will perform several sensitivity analyses and negative control analyses, such as restricting the population to women with singleton pregnancies, excluding individuals who had undergone in vitro fertilization (IVF), and considering those women who were prescribed herbal medicines during the middle and late stages of pregnancy as the negative exposure control group.

Enrollment

200,000 estimated patients

Sex

Female

Ages

15 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pregnancies registered at REPRESENT and underwent live births between January 2013 and December 2018 were included.

Exclusion criteria

  • (1) those with the first antenatal visit occurring after 20 gestational weeks, (2) those without timing records of the last menstrual period or delivery dates, (3) those with known factors related to birth defects (e.g.,syphilis positive, epilepsy), (4) those prescribed known medications associated with birth defects (e.g.,dezocine, diazepam).

Trial design

200,000 participants in 1 patient group

Drug exposure
Description:
Herbal medicines
Treatment:
Drug: Herbal medicines (e.g., Yunkang granules, Duzhong granules)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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