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A comparison of azithromycin and ofloxacin in the treatment of typhoid in adult patients in Laos

Completed
Conditions
Typhoid fever
Infections and Infestations
Registration Number
ISRCTN66534807
Lead Sponsor
niversity of Oxford (UK)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
88
Inclusion Criteria

1. Adult (more than or equal to 15 years, either sex) non-pregnant patients with suspected or blood culture proven typhoid
2. Fever more than 37.5 °C
3. Informed written consent to the study
4. Able to stay in hospital for seven days
5. Able to take oral medication
6. Body weight more than 40 kg
7. Likely to be able to complete six months follow up
8. None of the exclusion criteria

Exclusion Criteria

1. Known hypersensitivity to ofloxacin or azithromycin
2. Administration of chloramphenicol, co-trimoxazole, ampicillin, azithromycin or a fluoroquinolone during the previous week
3. Pregnancy or breast feeding
4. Contraindications to ofloxacin or azithromycin
5. Evidence for severe typhoid

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome measures are fever clearance, cure rate, relapse rate and S. typhi stool carriage rate.
Secondary Outcome Measures
NameTimeMethod
o secondary outcome measures
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