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Maternal Use of Antibiotics and the Risk of Congenital Malformations

S

Sichuan University

Status

Active, not recruiting

Conditions

Congenital Malformations

Treatments

Drug: Different categories of antibiotics

Study type

Observational

Funder types

Other

Identifiers

NCT06770465
Antibiotics and BDs

Details and patient eligibility

About

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.

Enrollment

850,000 patients

Sex

Female

Ages

14 to 65 years old

Volunteers

No Healthy Volunteers

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.

Trial design

850,000 participants in 2 patient groups

Use of antibiotics during pregnancy in FAERS and CVAR databases
Description:
When using the publicly available spontaneous adverse event reporting databases FAERS and CVAR, the exposure group consists of reports of adverse events in pregnant individuals who used different types of antibiotics, and the control group consists of other adverse event reports in which no antibiotics were used.
Treatment:
Drug: Different categories of antibiotics
Use of antibiotics during pregnancy in a cohort in Xiamen, China
Description:
When using the pregnant women cohort data from Xiamen, China, the exposure group consists of pregnant individuals who used the target antibiotics of interest, while the control group is either those who did not use any antibiotics (blank control) or those who used penicillin (positive control).
Treatment:
Drug: Different categories of antibiotics

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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