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Sayana-Uniject Volumetric Delivery

This study has been completed.
Information provided by:
Pfizer Identifier:
First received: December 16, 2010
Last updated: February 16, 2011
Last verified: February 2011

December 16, 2010
February 16, 2011
May 2010
June 2010   (Final data collection date for primary outcome measure)
Weight of drug suspension delivered (estimated by change in mass of the Uniject(TM) delivery system). [ Time Frame: Visit 1 ]
Same as current
No Changes Posted
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Sayana-Uniject Volumetric Delivery
Quantitative Determination of the Volume of Suspension Delivered Via the Uniject Delivery System Following Simulated Subcutaneous Injection by Healthcare Professionals Into a Synthetic Subcutaneous Injection Training Device
The purpose of this study is to determine the volumetric delivery of the Uniject.
Observe subjects deliver the drug None used
Time Perspective: Prospective
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Non-Probability Sample
Volume Delivery.
Other: Uniject
single use container
Group 1
All subjects
Intervention: Other: Uniject
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
June 2010
June 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Nurses

Exclusion Criteria:

  • Non-nurses
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
Contact information is only displayed when the study is recruiting subjects
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Director, Clinical Trial Disclosure Group, Pfizer, Inc.
Not Provided
Study Director: Pfizer Call Center Pfizer
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP