Actively Recruiting

Age: 6Months +
All Genders
NCT06821282

Surveillance of AMR in DRC

Led by University of Oxford · Updated on 2025-02-20

210

Participants Needed

1

Research Sites

46 weeks

Total Duration

On this page

Sponsors

U

University of Oxford

Lead Sponsor

U

University of Kinshasa

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study addresses knowledge gaps regarding antimicrobial resistance (AMR) in sub-Saharan Africa, focusing on evaluating the feasibility of AMR surveillance and enhancing local research capacity. Conducted at a general referral hospital in semirural Kinshasa, DRC, the study will investigate bacterial infections, their resistance profiles, and related risk factors, including co-infections such as malaria.

CONDITIONS

Official Title

Surveillance of AMR in DRC

Who Can Participate

Age: 6Months +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients older than six months
  • Patients with clinically suspected bloodstream infection at hospital admission
  • Patients hospitalized for less than 48 hours
  • Patients or their caregivers/legal guardians must provide written consent to participate
Not Eligible

You will not qualify if you...

  • Patients with a significant history of healthcare exposure
  • Patients with contraindications for phlebotomy as determined by clinician judgment

AI-Screening

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Trial Site Locations

Total: 1 location

1

Kinshasa, Democratic Republic of Congo, Kinshasa School of Public Health

Kinshasa, Democratic Republic of the Congo, BP 11850

Actively Recruiting

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Research Team

C

Caterina Fanello, Dr.

CONTACT

M

Marie Onyamboko, Prof

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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