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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01298479

Enrollment

Registered

2011-02-17

Start date

2010-05-31

Completion date

2010-06-30

Last updated

2018-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Volume Delivery

Keywords

volume delivery

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

Interventions

OTHERUniject

single use container

Study design

Observational model

OTHER

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

Inclusion criteria

* Nurses

Exclusion criteria

* Non-nurses

Design outcomes

Primary

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

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026