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Impact of Reducing Colistin Use on Colistin Resistance in Humans and Poultry in Indonesia (COINCIDE)

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Erasmus University

Status

Not yet enrolling

Conditions

Antimicrobial Resistance
Colonization, Asymptomatic
Mcr-1
Colistin

Treatments

Other: screening

Study type

Observational

Funder types

Other

Identifiers

NCT05960084
22-03-0255

Details and patient eligibility

About

Colistin (polymyxin E) is considered a last resort antimicrobial for treatment of infections with multidrug- resistant bacteria, classified by WHO as 'highest prioritized, critically important for human medicine'. WHO suggests to ban or highly restrict its use in animals. In Indonesia, colistin resistance in human Escherichia coli isolates is poorly characterized as it requires specific non-routine tests. Presence of colistin resistance in E. coli in poultry resulted in a ban for livestock in Indonesia in 2020. However, colistin is still suspected to be routinely used in humans in multiple settings but the reasons for these practices are poorly understood. The ban on colistin use in livestock offers a unique opportunity to assess the impact of this intervention on colistin resistance in humans and animals, and how a One Health perspective can strengthen this intervention. This project aims to: i) determine phenotypic and genotypic colistin resistance in E. coli from humans and poultry in Indonesia; ii) assess the impact of the colistin ban on resistance in E. coli in animals and humans; iii) estimate the transmission of colistin resistance between animals and humans; iv) study colistin use and perceptions at the community level; and v) expand the initial colistin ban in the animal production sector into an integrative multi-sectorial One Health intervention, which will be designed and implemented using a community participatory approach. This project will provide a strong scientific basis to AMR policies in Indonesia, with great significance across Southeast Asia.

Enrollment

803 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All individuals with age >= 18 years old, that are willing to participate

Exclusion criteria

  • Vomiting and/or diarrhea

Trial contacts and locations

1

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Central trial contact

Anis Karuniawati, MD PhD

Data sourced from clinicaltrials.gov

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