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The purpose of this study is to determine the volumetric delivery of the Uniject.
Observe subjects deliver the drug None used
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1 | All subjects |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Uniject | Other | single use container |
|
| Measure | Description | Time Frame |
|---|---|---|
| Weight of drug suspension delivered (estimated by change in mass of the Uniject(TM) delivery system). | Visit 1 |
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Inclusion Criteria:
Exclusion Criteria:
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nurses
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| Name | Affiliation | Role |
|---|---|---|
| Pfizer CT.gov Call Center | Pfizer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Pfizer Investigational Site | Brussels | B-1070 | Belgium |
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| Label | URL |
|---|---|
| To obtain contact information for a study center near you, click here. | View source |
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