Sayana-Uniject Volumetric Delivery

Completed

• Conditions: Volume Delivery
• Interventions: Other: Uniject

• Registration Number: NCT01298479
• Lead Sponsor: Pfizer

Brief Summary

The purpose of this study is to determine the volumetric delivery of the Uniject.

Detailed Description

Observe subjects deliver the drug None used

Study Timeline

• Study Start: 2010-05
• Primary Completion: 2010-06
• Study Completion: 2010-06
• Study First Submitted: 2010-12-16
• Study First Submitted QC: 2011-02-16
• Study First Posted: 2011-02-17
• Status Verified: 2018-12
• Last Update Submitted: 2018-12-05
• Last Update Posted: 2018-12-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• Nurses

Exclusion Criteria

• Non-nurses

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Group 1	Uniject	All subjects

Primary Outcome Measures

Name	Time	Method
Weight of drug suspension delivered (estimated by change in mass of the Uniject(TM) delivery system).	Visit 1

Trial Locations

Locations (1)

Pfizer Investigational Site; 🇧🇪 Bruxelles, Belgium