NCT02093494View on ClinicalTrials.gov

Study to Evaluate the Effectiveness of the Initial Specimen Diversion Device When Collected Through Peripheral Intravenous Catheters

NATerminatedINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

May 31, 2015

Study Completion Date

May 31, 2015

Conditions
Septicemia
Interventions
DEVICE

Initial Specimen Diversion Device (ISDD)

PROCEDURE

Lab standard practice (LSP)

DEVICE

Peripheral Intravenous Catheters (PIVC)

Trial Locations (1)

02115

Brigham and Women's Hospital, Boston

Sponsors
All Listed Sponsors
lead

Magnolia Medical Technologies, Inc.

INDUSTRY

NCT02093494 - Study to Evaluate the Effectiveness of the Initial Specimen Diversion Device When Collected Through Peripheral Intravenous Catheters | Biotech Hunter | Biotech Hunter