Azithromycin, With or Without Loperamide, to Treat Travelers' Diarrhea
Diarrhea
About this trial
This is an interventional treatment trial for Diarrhea focused on measuring Diarrhea, Travel, Travelers' diarrhea, Azithromycin, Loperamide, Treatment, Antibiotic
Eligibility Criteria
Inclusion Criteria: Eligible subjects included men or women, recently arrived in Mexico, at least 18 years of age, who developed acute diarrhea, which was defined as passage of 3 or more unformed stools in the preceding 24 hours accompanied by one or more signs or symptoms of enteric infection (e.g., nausea, vomiting, abdominal cramps, tenesmus, passage of grossly bloody stools or fecal urgency) with a duration of illness of less than or equal to 72 hours. Exclusion Criteria: Exclusion criteria included pregnancy, breast feeding, an unstable medical condition, taking two or more doses of an antidiarrheal medication in the 24 hours before enrollment or any number of doses of symptomatic therapy within 2 hours of enrollment, or receiving an antimicrobial drug with expected activity against enteric bacterial pathogens within 7 days prior to enrollment.
Sites / Locations
- University of Texas Enteric Disease Research Clinics
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Experimental
Azithromycin 500 mg plus Placebo
Azithromycin 1000 mg plus Placebo
Azithromycin 500 mg plus Loperamide
a single 500 mg dose of Azitrhomycin at the start of treatment; a single loading dose of placebo at the start of treatment and then a dose of placebo after each loose stool
a single 1000 mg dose of Azitrhomycin at the start of treatment; a single loading dose of placebo at the start of treatment and then a dose of placebo after each loose stool
a single 500 mg dose of Azitrhomycin at the start of treatment; a single 4 mg loading dose of Loperamide at the start of treatment and then 2 mg Loperamide after each loose stool