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NCT06371261Active, not recruiting

Pathogenicity of Species of the Achromobacter Genus in Patients From Reunion Island With Cystic Fibrosis

Pathogenicity of Species of the Achromobacter Genus in Patients With Cystic Fibrosis: a Prospective Multicentre Exploratory Study of a Cohort in Réunion Island.

Source: ClinicalTrials.gov · Last updated 4 May 2026

Brief summary (registry, in English)

The pathogenicity of Achromobacter bacteria is not yet well established, but studies show a decline in respiratory function and an increase in mortality associated with chronic colonisation, making it possible to classify the Achromobacter genus as an emerging pathogen in cystic fibrosis. It is possible that certain species or clones are more virulent or resistant, requiring the adaptation of measures to prevent cross-transmission in the centres concerned. However, until now, the identification of Achromobacter species has involved the use of molecular biology techniques that are not routinely applicable in diagnostic laboratories, limiting studies and the collection of epidemiological data. Recently, a database using MALDI-TOF mass spectrometry has been built for rapid and accurate species identification. In view of the local epidemiology and the current lack of data, it would be necessary and interesting to use this tool to study a cohort of cystic fibrosis patients in Réunion island (North and South sites) to see whether one species has a greater clinical impact than another (pathogenicity), and/or is more responsible for chronic colonisation.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
17 (actual)
First submitted
2 Apr 2024
Start date
12 Mar 2024
Primary completion date
19 Mar 2027
Lead sponsor
Centre Hospitalier Universitaire de la Réunion
NCT number
NCT06371261

What you commit to

  • Study type: Observational
  • Participants enrolled: 17
  • From 12 Mar 2024 to the primary completion date, 19 Mar 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients without cystic fibrosis.
  • Patients with cystic fibrosis but no Achromobacter-positive ECBC during the study inclusion period

Who the study is looking for

  • Minor or major cystic fibrosis patients
  • Patients with at least one sputum cytobacteriological test positive for Achromobacter spp. during the inclusion period.
  • Patients living in La Réunion island.
  • Patients for whom a non-opposition was obtained orally (if applicable from both one of the child's legal guardians and the child him/herself)

Sex: All

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU la Réunion North
Coordinator of this site? Confirm its status
Saint-DenisRéunionUnknown status
CHU la Réunion South
Coordinator of this site? Confirm its status
Saint-PierreRéunionUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.