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Clinical Trials in China / NCT06770465
Active, not recruiting Observational

Maternal Use of Antibiotics and the Risk of Congenital Malformations

NCT06770465 · tracked via the Priya Life Science China tracker
Sponsor
West China Hospital
Phase
Observational
Started
2024-06-01
Last updated
2025-01-13

Condition(s) studied

Congenital Malformations

Investigational drug(s) / intervention(s)

Different categories of antibiotics

Different categories of antibiotics: Use of different categories of antibiotics during pregnancy, such as quinolones and macrolides.

Study summary

Antibiotics are widely used during pregnancy to prevent or treat infections, yet concerns remain regarding their fetal safety. Drawing on data from spontaneous reporting databases and cohort studies, this study aims to explore potential associations between exposure to various antibiotic classes during pregnancy and congenital malformations.

Data were collected from publicly available reports in the U.S. Food and Drug Administration's Adverse Event Reporting System (FAERS), the Canada Vigilance Adverse Reaction (CVAR) database, and a population-based retrospective cohort in Xiamen, China. By applying multiple signal detection methods, we identified potential risk signals linking different antibiotic classes to organ-system-specific congenital malformations. For antibiotics showing positive signals, we further utilized a pregnancy medication cohort in Xiamen and applied causal inference techniques to estimate the adjusted relative risk of congenital malformations associated with first-trimester exposure to these antibiotics. Several sensitivity analyses-including both negative- and positive-control analyses-will also be performed.

Eligibility

Sex
FEMALE
Min age
14 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * For the spontaneous reporting data study, all adverse reactions reported by mothers were included. For the cohort study, all Xiamen pregnant women registered in the cohort were included Exclusion Criteria: * For studies using spontaneous reporting data, all adverse reaction reports unrelated to pregnant or postpartum women-including those occurring during the lactation period-were excluded. For cohort studies, pregnant women who were lost to follow-up were excluded, and pregnant women who were exposed to factors known to be associated with congenital malformations were excluded.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The West China Hospital of Sichuan university Chengdu Sichuan

More West China Hospital trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06770465 on ClinicalTrials.gov ↗ ← All trials in China