Typhoid Fever Clinical Trial
Official title:
Typhoid Fever: Combined vs. Single Antibiotic Therapy. A Prospective Randomized Controlled Study in Nepal.
The current study goal is to examine the effect of Cephalosporins, Azithromycin and the
combination of both on typhoid fever therapy in endemic population.
The investigator's hypothesize that the combination of azithromycin and ceftriaxone may
prove superior to each drug, ceftriaxone or azithromycin, alone.
Typhoid Fever is a highly prevalent infection in the Indian subcontinent. Due to multidrug
resistant strains in these areas, third generation cephalosporins, such as ceftriaxone, are
the treatment of choice. However, the latter regimen exhibits a slow response with mean time
of 5 to 7 days or even longer to defervescence, which could be attributed to poor
penetration capability of the drug into cells, and thus difficulty to eradicate the bacteria
from the intracellular niche.
Attempts have been made to overcome this setback by introducing alternative antibiotic
regimens, such as azithromycin. However studies comparing between azithromycin and a
third-generation cephalosporin for the treatment of typhoid fever in adult population in the
Indian subcontinent are lacking.
Over the last few years our approach towards non-immunized travelers, who acquired typhoid
fever in the Indian subcontinent, was to administer a combination therapy of intravenous
ceftriaxone with oral azithromycin. The rationale of this dual regimen was its
pharmacokinetic profile, which suggests a complimentary action of the two agents -
ceftriaxone on the extracellular compartment and azithromycin on the intracellular
compartment. Moreover, in our clinical experience, preliminary published data has proven
combination therapy significantly superior to ceftriaxone alone albeit in a small group of
travelers.
In the current study the investigators intend to compare the efficacy of ceftriaxone vs.
azithromycin and vs. combined therapy of both agents for the treatment of uncomplicated
typhoid fever in terms of time to defervescence.
4 different treatment strategies will be examined (as mentioned in the arm section). All
participants will be checked for vital signs, will undergo physical examination, ECG,
laboratory testing, blood, urine and stool culture and tests for susceptibility to
antibiotics.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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