Clinical Trials Directory

Trials / Completed

CompletedNCT01467934

FeverText: Assessing Fever Rates After Vaccination During the 2011-12 Influenza Season Using Text Messaging

FeverText: Assessing Fever Rates After Influenza and Pneumococcal Vaccination During the 2011-12 Influenza Season Using Text Messaging

Status
Completed
Phase
Study type
Observational
Enrollment
530 (actual)
Sponsor
Columbia University · Academic / Other
Sex
All
Age
6 Months – 23 Months
Healthy volunteers
Not accepted

Summary

In this study, the investigators will prospectively assess fever rates and other associated vaccine adverse events in 6-23 month old patients during days 0-7 after administration of trivalent inactivated influenza vaccine (TIV) and 13-valent pneumococcal conjugate vaccine (PCV13) concomitantly compared to those who receive trivalent inactivated influenza vaccine (TIV) or 13-valent pneumococcal conjugate vaccine (PCV13) administered non-concomitantly. The investigators hypothesize that fever rates will be significantly higher during the 0-1 days after vaccination when inactivated influenza vaccine (TIV) and 13-valent pneumococcal conjugate vaccine (PCV13) are given concomitantly than when TIV or PCV13 is administered non-concomitantly.

Conditions

Timeline

Start date
2011-11-01
Primary completion
2012-04-01
Completion
2012-06-01
First posted
2011-11-09
Last updated
2014-07-21
Results posted
2014-07-21

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01467934. Inclusion in this directory is not an endorsement.