Prospective Comparison of Ampicillin / Amoxicillin Versus Ceftriaxone for the Treatment of Salmonella Infections in AIDS Patients
Sponsor
University of Southern California (Other)
Overall Status
Completed
CT.gov ID
NCT00002052
Collaborator
(none)
1
Study Details
Study Description
Brief Summary
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.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Study Design
Study Type:
Interventional
Primary Purpose:
Treatment
Official Title:
Prospective Comparison of Ampicillin / Amoxicillin Versus Ceftriaxone for the Treatment of Salmonella Infections in AIDS Patients
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 0 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Los Angeles County - USC Med Ctr | Los Angeles | California | United States | 90033 |
Sponsors and Collaborators
- University of Southern California
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00002052
Other Study ID Numbers:
- 019A
First Posted:
Aug 31, 2001
Last Update Posted:
Jun 24, 2005
Last Verified:
Aug 1, 1989
Keywords provided by ,
,
Additional relevant MeSH terms: