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Sayana-Uniject Volumetric Delivery

This study has been completed.
Sponsor:
Information provided by:
Pfizer
ClinicalTrials.gov Identifier:
NCT01298479
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 ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01298479 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
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

Observational
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

nurses

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 ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
25
June 2010
June 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Nurses

Exclusion Criteria:

  • Non-nurses
Both
18 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Belgium
 
NCT01298479
A6791034
No
Director, Clinical Trial Disclosure Group, Pfizer, Inc.
Pfizer
Not Provided
Study Director: Pfizer CT.gov Call Center Pfizer
Pfizer
February 2011

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