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Sayana-Uniject Volumetric Delivery

Pfizer logo

Pfizer

Status

Completed

Conditions

Volume Delivery

Treatments

Other: Uniject

Study type

Observational

Funder types

Industry

Identifiers

NCT01298479
A6791034

Details and patient eligibility

About

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

Full description

Observe subjects deliver the drug None used

Enrollment

25 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Nurses

Exclusion criteria

  • Non-nurses

Trial design

25 participants in 1 patient group

Group 1
Description:
All subjects
Treatment:
Other: Uniject

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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