Antibiotic Concentrations After MassivE Transfusion Study

Recruiting Observational Study
Adverse Effects in the Therapeutic Use of Other and Unspecified Agents Affecting Blood Constituents
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
417 (estimated)
Sponsor
Brooke Army Medical Center · Federal
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About This Trial
Combat and civilian trauma frequently result in open wounds that are at risk for infection. Data from the Department of Defense Trauma Registry demonstrate that 74% of combat trauma casualties have an open wound. The Committee on Tactical Combat Casualty Care, the Prolonged Field Care Working Group, and the Joint Trauma System clinical practice guidelines recommend antibiotic prophylaxis for open …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Receives ampicillin/sulbactam, cefazolin, cefepime, ceftriaxone, clindamycin, ertapenem, levofloxacin, metronidazole or pipercillin/tazobactam at any dose * Hospitalized or anticipated hospital admission Exclusion Criteria: * Received the same antibiotic within the past 5 ha…
Contacts

Steven G Schauer, DO

2109160808

steven.g.schauer.mil@army.mil

CONTACT

Jessica Mendez, MS

jessica.mendez32.ctr@health.mil

CONTACT