Lassa Fever |
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Clinical Trial: Treatment of neutropenic patients with fever who are suspected to have a gram positive infection (a specific kind of bacteria)
This study has been completed.
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Purpose
This study will treat patients who have fever and neutropenia (after cancer chemotherapy) that is possibly due to a specific bacteria (gram positive bacteria)
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Neutropenia Fever Gram-Positive Bacterial Infections Neoplasms | Drug: Antibiotic Drug: Vancomycin | Phase III |
MedlinePlus related topics: Bacterial Infections; Blood and Blood Disorders; Cancer; Cancer Alternative Therapy; Fever
Study Type: Interventional
Study Design: Treatment
Eligibility
Ages Eligible for Study: 13 Years and above, Genders Eligible for Study: Both
Criteria
Other specific inclusion/exclusion criteria may apply. In order to determine eligibility, further examination by the investigator is necessary.
Inclusion Criteria:
- Patients must have neutropenia (ANC less than 500) with fever (oral temp 38.3 C).
- Patients must have a cancer with recent chemotherapy and risks factors for gram positive infections.
Exclusion Criteria:
- Patients with fever due to known causes.
- Patients with HIV.
- Patients with recent bone marrow transplant.
- Patients with an infected indwelling catheter that cannot be removed.
- Patients who have received more than one day of another antibiotic before entering the trial.
- Patients with endocarditis, osteomyelitis, meningitis, CNS infections.
Location Information
California
Research Center, San Diego, California, 92134, United States
Research Center, Los Angeles, California, 90033, United States
Research Center, Orange, California, 92868, United States
Florida
Research Center, Miami, Florida, 33136, United States
Illinois
Research Center, Springfield, Illinois, 62701, United States
Research Center, Maywood, Illinois, 60153, United States
Kentucky
Research Center, Lexington, Kentucky, 40536, United States
Massachusetts
Research Center, Worcester, Massachusetts, 01655, United States
Michigan
Research Center, Kalamazoo, Michigan, 49001, United States
New Jersey
Research Center, Perth Amboy, New Jersey, 08861, United States
New York
Research Center, Bronx, New York, 10467-2490, United States
Ohio
Research Center, Youngstown, Ohio, 44501, United States
Tennessee
Research Center, Jackson, Tennessee, 38301, United States
Texas
Research Center, Houston, Texas, 77030-4211, United States
Research Center, Houston, Texas, 77030, United States
Virginia
Research Center, Richmond, Virginia, 23249, United States
Research Center, Falls Church, Virginia, 22042, United States
Research Center, Richmond, Virginia, 23294, United States
Washington
Research Center, Tacoma, Washington, 98405, United States
Wisconsin
Research Center, Milwaukee, Wisconsin, 53226, United States
Puerto Rico
Research Center, Hato Rey, 00985, Puerto Rico
More Information
Record last reviewed: March 2004
Last Updated: October 13, 2004
Record first received: May 3, 2002
ClinicalTrials.gov Identifier: NCT00035425
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Arenaviruses (MayoClinic)

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