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NCT00401700 Clinical Trial

Influenza Vaccine Postpartum Questionnaire

Pregnancy Clinical Trial

Official title:
Acceptability and Feasibility of Influenza Vaccine Administration on the Post-partum Floor Prior to Discharge Home During Flu Season

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00401700
Other study ID # 06-190
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2006
Est. completion date July 2009

Study information
Verified date February 2019
Source St. Michael's Hospital, Toronto
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this trial is to assess the knowledge and attitudes of post-partum women regarding influenza and the use of the influenza vaccine in pregnancy.

Description:

Women on our post-partum floor will be approached to complete a questionnaire which will assess their knowledge and attitudes regarding influenza and the use of the influenza vaccine in pregnancy. The study will take place over a 2-month period during influenza season, and at the time when the influenza vaccine becomes available.

Recruitment information / eligibility
Status Completed
Enrollment 150
Est. completion date July 2009
Est. primary completion date January 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- women admitted to the postpartum floor during the study period

Exclusion Criteria:

- inability to read or understand English

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Canada St. Michael's Hospital Toronto Ontario

Sponsors (1)
Lead Sponsor Collaborator
St. Michael's Hospital, Toronto

Country where clinical trial is conducted

Canada, 

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