Afluria Pregnancy Registry

Pregnancy Clinical Trial

Official title:

A Prospective Observational Safety Study on Pregnancy Outcomes in Women Immunized With Afluria, a Seasonal Influenza Vaccine, During Pregnancy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03442582
• Other study ID #: CSLCT-OBS-17-15
• Status: Completed
• Start date: September 8, 2017
• Est. completion date: September 14, 2021

Study information

• Verified date: February 2022
• Source: Seqirus
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The study is a population based prospective cohort study designed to collect data on pregnancy outcomes and events of interest among women immunized with Afluria during pregnancy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 490
• Est. completion date: September 14, 2021
• Est. primary completion date: September 14, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

Enrollment and data collection will be coordinated through a coordination center (CC). The minimum eligibility criteria required for enrollment are as follows:

• Sufficient information to confirm that the exposure of interest occurred during pregnancy and at which date.

• Sufficient information to determine whether it concerns a prospectively enrolled subject, since retrospective cases are ineligible for enrollment.

• Reporter (e.g. HCP) contact information to allow for follow-up

Exclusion Criteria:

• N/A

Related Conditions & MeSH terms

• Birth Defect
• Congenital Abnormalities
• Influenza, Human
• Pregnancy

Intervention

Biological:
• Afluria Influenza Vaccine
Afluria is a seasonal influenza vaccine Vaccine exposure in routine care (no vaccination per protocol)

Locations

Country	Name	City	State
United States	Syneos Health	Wilmington	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Seqirus

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety Objective: Number of cases for pregnancy outcomes among women immunized as part of routine care with Afluria, a seasonal influenza vaccine, during pregnancy.	Pregnancy outcomes will be reported as one of the following: live birth, stillbirth, spontaneous abortion and elective termination	From time of enrollment during pregnancy to time of delivery or pregnancy termination; a follow-up period of up to 40 weeks
Primary	Safety Objective: Number of cases with events of major congenital malformations among women immunized as part of routine care with Afluria, a seasonal influenza vaccine, during pregnancy.		From time of enrollment during pregnancy to time of delivery or pregnancy termination; a follow-up period of up to 40 weeks
Primary	Safety Objective: Number of cases of events of preterm birth among women immunized as part of routine care with Afluria, a seasonal influenza vaccine, during pregnancy.		From time of enrollment during pregnancy to time of delivery or pregnancy termination; a follow-up period of up to 40 weeks
Primary	Safety Objective: Number of cases of events of low birth weight among women immunized as part of routine care with Afluria, a seasonal influenza vaccine, during pregnancy.		From time of enrollment during pregnancy to time of delivery or pregnancy termination; a follow-up period of up to 40 weeks