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H1N1 Vaccine in Pregnancy: a Registry for the Fall and Winter of 2009

H1N1 Vaccine in Pregnancy: a Registry for the Fall and Winter of 2009

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01374009
Enrollment
504
Registered
2011-06-15
Start date
2010-04-30
Completion date
2012-12-31
Last updated
2017-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vaccine Exposure During Pregnancy

Brief summary

The goal of this study it to rapidly create a brief registry of pregnant women who receive the H1N1 vaccine in Ontario, British Columbia, and Nova Scotia during the pandemic H1N1 2009/2010 influenza season.

Detailed description

For Part 1, a brief amount of data will be collected on each woman at the time of her vaccination. These data will be filled out on a single data collection sheet by her Obstetrics Clinic physician or nurse, which will be completed at the time of her vaccination. For Part 2, after a woman's expected delivery date, data sources will be used for participants. Two groups of non-vaccinated controls will be derived from the provincial perinatal databases: 1. The active non-vaccinated controls will be recruited from the concurrent year, matched to women who were vaccinated in 2009/2010. For each of the three perinatal databases, 5 non-vaccinated active controls will be matched by maternal age +/- 3 years, same-hospital delivery, and delivery date +/- 7 days. 2. The passive non-vaccinated controls will be derived from the preceding year (i.e., 2008). For each of the three perinatal databases, 5 non-vaccinated passive controls will be matched by maternal age +/- 3 years, same-hospital delivery, and delivery date +/- 7 days. For women who delivered in Ontario, the Niday Perinatal Database will be used. (https://www.nidaydatabase.com/info/index.shtml). For women who deliver in British Columbia, their data will be linked to the British Columbia Perinatal Database Registry (http://www.bcphp.ca/Database%20Content.htm). Women who deliver in Nova Scotia will be linked to Nova Scotia Atlee Perinatal Database (http://rcp.nshealth.ca/rcp\_3347.html). Information that will be obtained is as follows: * Actual delivery date (DD/MM/YYYY) * Number of infants delivered * Mode of delivery (vaginal for Caesarean) * Liveborn or stillborn * Presence of a congenital anomaly * Presence of intrauterine growth restriction or small-for-gestational age birthweight * Presence of a neonatal infection * Presence of neonatal sepsis * Need for ventilation of the neonate * Need for Neonatal Intensive Care of the Neonate. For Part 3, between 18-24 months after a woman's actual delivery date, a woman may be telephoned at her home to ask her about the health and developmental milestones of her baby. This phase may or may not be done, but consent will be obtained nonetheless.

Interventions

None listed

Sponsors

Li Ka Shing Foundation
CollaboratorOTHER
PHAC/CIHR Influenza Research Network
CollaboratorOTHER_GOV
Dalhousie University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Received the H1N1 vaccine during pregnancy

Exclusion criteria

* None

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026