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.