Ciprofloxacin for the Prevention of Meningococcal Meningitis 2018

NCT03431675 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2019-08-14

No results posted yet for this study

Summary

The trial is an interventional, cluster-randomized trial to assess the impact of oral ciprofloxacin for household and community contacts of meningitis cases on the incidence of meningitis during an epidemic.

The trial contains a nested sub-study ("resistance study") to assess the effect of a single dose of ciprofloxacin on the prevalence of fluoroquinolone-resistant enterobacteriaceae in the study area.

Conditions

  • Meningitis, Meningococcal

Interventions

DRUG

Ciprofloxacin

Single-dose oral ciprofloxacin

Sponsors & Collaborators

  • Medecins Sans Frontieres, Netherlands

    collaborator OTHER
  • Epicentre

    lead OTHER

Principal Investigators

  • Rebecca F GRAIS, PhD · Epicentre

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-01
Primary Completion
2019-06-30
Completion
2019-12-31

Countries

  • Niger

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03431675 on ClinicalTrials.gov