Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Los Angeles, California 90033


Purpose:

To compare the effectiveness of standard treatment with parenteral ampicillin and oral amoxicillin compared to initial daily therapy with ceftriaxone followed by 3 times weekly suppressive treatment for salmonella infections in AIDS patients.


Criteria:

Exclusion Criteria Co-existing Condition: Patients with the following are excluded: - Type I hypersensitivity to beta-lactam antibiotics. - Not expected to survive 12 weeks. - In a coma or with other central nervous system (CNS) impairment. Patients with the following are excluded: - Type I hypersensitivity to beta-lactam antibiotics. - Not expected to survive 12 weeks. - In a coma or with other central nervous system (CNS) impairment. Prior Medication: Excluded within 48 hours of study entry: - Treatment with an antibiotic active in vitro against Salmonella. HIV infection, AIDS, or AIDS related complex (ARC). - Salmonella bacteremia or positive stool culture in patient with 3 or more stools per day.


NCT ID:

NCT00002052


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Los Angeles, California 90033
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 22, 2017

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.