The Cymbalta Pregnancy Registry

NCT01074151 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 144

Last updated 2022-07-18

No results posted yet for this study

Summary

The Cymbalta Pregnancy Registry is a U.S. based Registry designed to monitor women who are exposed to Cymbalta (duloxetine) during pregnancy. This is an observational, exposure-registration and follow-up registry.

Conditions

  • Pregnancy

Interventions

DRUG

duloxetine

any exposure to duloxetine that occurred during pregnancy

Sponsors & Collaborators

Principal Investigators

  • INC Research, LLC · Syneos Health

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2021-07-26
Completion
2021-07-26

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01074151 on ClinicalTrials.gov