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HIV InfectionsNCT00002052

Prospective Comparison of Ampicillin / Amoxicillin Versus Ceftriaxone for the Treatment of Salmonella Infections in AIDS Patients

A study testing Ceftriaxone sodium, Ampicillin sodium and Amoxicillin trihydrate in people with HIV Infections and Salmonella Infections, run by University of Southern California at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
HIV Infections, Salmonella Infections
What is being tested?
Ceftriaxone sodium, Ampicillin sodium and Amoxicillin trihydrate
How many people
Not given
Where
1 siteUnited States
Study dates
Start not givento not given
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • 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:
Show all 14Show fewer
  • 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.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Los Angeles County - USC Med Ctr

    Los Angeles, California, 90033

Other trials in United States

About this study

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.

Being tested
Ceftriaxone sodium, Ampicillin sodium, Amoxicillin trihydrate
Keywords
Salmonella Infections, AIDS-Related Opportunistic Infections, Acquired Immunodeficiency Syndrome, Amoxicillin, Ceftriaxone
Medical subject headings
HIV Infections, Salmonella Infections, AIDS-Related Opportunistic Infections, Acquired Immunodeficiency Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Ceftriaxone sodiumDrug

  • Ampicillin sodiumDrug

  • Amoxicillin trihydrateDrug

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Aug 2001 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
IDs, dates and publications
ClinicalTrials.gov ID
NCT00002052
Sponsor's protocol ID
019A
Status last verified
Aug 1989
First submitted
2 Nov 1999
Last updated
24 Jun 2005
Results posted
No

Questions about this trial

What is this clinical trial studying?

A study testing Ceftriaxone sodium, Ampicillin sodium and Amoxicillin trihydrate in people with HIV Infections and Salmonella Infections, run by University of Southern California at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Jun 2005. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2005.

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