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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06048276
Enrollment
200000
Registered
2023-09-21
Start date
2023-01-01
Completion date
2024-12-31
Last updated
2024-05-07

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

Conditions

Birth Defects, Drug Exposures, Pregnancy

Keywords

Herbal medicines, Birth defects, Drug exposures, Cohort study

Brief summary

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.

Detailed 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.

Interventions

DRUGHerbal medicines (e.g., Yunkang granules, Duzhong granules)

Herbal medicines (e.g., Yunkang granules, Duzhong granules) exposure at the early gestation.

Sponsors

Xiamen Health Commission
CollaboratorUNKNOWN
Xiamen Health and Medical Big Data Center
CollaboratorUNKNOWN
West China Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 60 Years
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
Overall birth defects (excluding chromosomal malformations)From conception to 42 days after deliveryNumber of births with birth defects

Secondary

MeasureTime frameDescription
National monitored 23 main types of birth defectsFrom conception to 42 days after deliveryNumber of births with 23 major births defects defined by National Health Standard Criteria in the China national universal surveillance system

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026