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Multidrug Resistant Shigella Infection in Bangladesh

Clinical and Microbiologic Outcomes in Patients Treated for Multidrug-resistant Shigella Infections in Dhaka, Bangladesh

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03778125
Enrollment
2000
Registered
2018-12-19
Start date
2018-12-13
Completion date
2020-01-31
Last updated
2019-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diarrhea, Shigella

Keywords

multidrug resistant

Brief summary

The purpose of this project is to systematically collect clinical and nutritional outcomes information on patients treated for Shigella infection so that physicians and clinical laboratories can better define which Shigella infections are resistant to antibiotics and which are susceptible, focusing on azithromycin a last-line drug to treat drug resistant Shigella

Detailed description

2000 suspected Shigella cases will be recruited from International Centre for Diarrhoeal Disease Research hospital, Dhaka who are presenting with diarrhea at the hospital. A stool sample will be collected from the participants after consenting by the study staff. Stool microscopy will be performed to see the white blood cells(WBC) and red blood cells (RBC). If WBC \> 10 HPF (4) with any RBC present, culture will be performed from this stool to identify Shigella. Such patients with invasive diarrhea are treated with azithromycin per local standard of care. Enrolled participant will be invited for further follow up when culture from the stool is Shigella positive. Minimal inhibitory concentration (MIC) testing of Shigella isolates and Molecular testing of Shigella isolates will be performed from Shigella cultures. This is an observational study. This study does not provide any treatment to the study participants; they will receive treatment as per International Centre for Diarrhoeal Disease Research Dhaka hospital guidelines. We will then examine the effect of the azithromycin minimal inhibitory concentration on clinical outcome.

Interventions

None listed

Sponsors

Centers for Disease Control and Prevention
CollaboratorFED
International Centre for Diarrhoeal Disease Research, Bangladesh
CollaboratorOTHER
University of Virginia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* diarrheal illness less than 96 hours duration * microscopic evidence of inflammatory diarrhea * plus mucus in stool * plus abdominal pain/cramps * Subject or parents or legal guardian willing to come for follow up at hospital or allow study staff for home visit * residence in Dhaka region * presentation during daytime hours

Exclusion criteria

• Not receiving treatment with azithromycin at enrolment

Design outcomes

Primary

MeasureTime frameDescription
Clinical outcome: resolution of diarrheaDay 5resolution of diarrhea as measured by the participant through a memory aid

Secondary

MeasureTime frameDescription
Microbiologic outcome: Shigella negative culturesDay 5Proportion shigella culture negative isolates
Proportion of patients that have complicationsday 5required hospitalization or have extraintestinal complications

Other

MeasureTime frameDescription
time to last unformed stoolDay 5duration of diarrhea in days
difference in invasion plasmid antigen H (ipaH)Day 5molecular detection of Shigella quantity
feverDay 5duration of fever in days
bloody stoolDay 5duration of bloody stool in days

Countries

Bangladesh

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026