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A Study to Assess Maternal and Fetal Outcomes After Taking Prucalopride During Pregnancy

Pregnancy Clinical Trial

Official title:
Observational Study to Assess Maternal and Fetal Outcomes Following Exposure to Prucalopride During Pregnancy

Clinical Trial Summary

This study will collect information on pregnant women diagnosed with constipation from their health care insurance claims records. It will include the following groups: - Those who took prucalopride. - Those who took other medicines for constipation. - Those who did not take any prescription medicines for constipation. The main aim of the study is to assess the risk of major birth defects with the mother's use of prucalopride during the first 3 months of pregnancy. The study uses existing health care insurance information; participants are not enrolled, treated, or required to visit the doctor during this study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04961840
Study type Observational
Source Takeda
Contact
Status Active, not recruiting
Phase
Start date January 1, 2022
Completion date December 1, 2025
View Details
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