Status:
COMPLETED
Effectiveness of Short-Course Versus Standard Antibiotic Therapy in ICU Patients
Lead Sponsor:
National Institutes of Health Clinical Center (CC)
Conditions:
Bacterial Infections
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
This study will compare two treatment strategies (standard versus short-course antibiotic therapy) for preventing resistant bacterial infection in patients in the intensive care unit (ICU). ICUs are t...
Detailed Description
This study will enroll subjects who have been hospitalized at least three days (on or after fourth day of hospital stay), who have new pulmonary infiltrates during their ICU stay and who are at low ri...
Eligibility Criteria
Inclusion
- INCLUSION CRITERIA:
- The study will be limited to the medical, surgical, neurosurgical, trauma, and general ICUs of the participating institutions. Burn ICUs are not eligible for this study.
- Subjects who meet all of the following criteria are eligible for enrollment into the study:
- Subject, or legal representative, has given written informed consent.
- Subject has developed a new pulmonary infiltrate (confirmed by radiology), after ICU admission.
- Subject has been hospitalized at least 3 days.
- CPIS less than or equal to 6.
- 18 years of age or older.
- EXCLUSION CRITERIA:
- Subjects who meet any of the following criteria are ineligible for participation in the study:
- Burn patients.
- Cystic fibrosis patients.
- Bone marrow or solid organ transplant patients.
- Neutropenia from any cause (absolute neutrophil count (ANC) \< 500), or likely to become neutropenic within 7 days.
- Known or suspected Human Immunodeficiency Virus (HIV) infection (HIV test is not required).
- Suspected or proven extrapulmonary infection site requiring antibiotic therapy.
- History of anaphylaxis to penicillin or cephalosporins.
- History of anaphylaxis to meropenem (any component of the formulation), or other carbapenems (e.g., imipenem).
- On systemic antibiotics for more than 7 consecutive days during the previous 30 days.
- Received more than two doses of systemic antibiotics within the past 24 hours (other than those used for surgical prophylaxis).
- Pregnant or lactating. (Women of childbearing potential must have a negative serum or urine pregnancy test within the 7 days prior to the first dose of antibiotics.)
- On mechanical ventilation for \> 7 consecutive days during the previous 30 days.
- Unlikely to survive past Day 7 of the study (as determined by the primary care team).
- Previous enrollment in this study.
Exclusion
Key Trial Info
Start Date :
August 11 2006
Trial Type :
INTERVENTIONAL
End Date :
May 22 2007
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00410527
Start Date
August 11 2006
End Date
May 22 2007
Last Update
July 2 2017
Active Locations (12)
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1
University of Alabama at Birmingham
Birmingham, Alabama, United States
2
Christiana Care Health Services
Newark, Delaware, United States, 19713
3
University of Miami
Miami, Florida, United States, 33101
4
University of Maryland, Baltimore
Baltimore, Maryland, United States, 21201-1595