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Diagnosis of Tuberculosis in Swiss Children

Study acronym: CITRUS
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Notable Primary completion date: Dec 2022 to Dec 2026
    • Study completion date: Dec 2022 to Dec 2028
    • Study description expanded, about 19 words
    • Study sites revised (8)
    v10
  2. Minor 2 versions Re-verified since Dec 10, 2020, no change to tracked fieldsv8-v9
  3. Notable Primary completion date: Apr 2019 to Dec 2022
    • Study completion date: Dec 2019 to Dec 2022
    • Study sites revised (8)
    v7
  4. Minor Study sites: 6 to 8v6
  5. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 6
    • Start date changed from estimate of May 2017 to May 12, 2017
    v5
Show 3 earlier versionsHide 3 earlier versions
  1. Notable Start date: Mar 27, 2017 to May 2017v4
  2. Minor Study description shortened, about 86 wordsv3
  3. Minor Secondary endpoints: details revised at 1 of 1 entryv2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
1. The primary objective is to improve the sensitivity of novel immunodiagnostic tests for detection of TB disease in children. 2. The secondary objective is to determine biomarkers that discriminate children with TB infection and disease.
Trial Details
NCT Number NCT03044509
Lead Sponsor University Children's Hospital Basel
Collaborators: Ospedale Regionale Bellinzona e Valli, Insel Gruppe AG, University Hospital Bern, University of Lausanne Hospitals, University Hospital, Geneva, Luzerner Kantonsspital, Cantonal Hospital of St. Gallen, University Children's Hospital, Zurich, Kantonsspital Aarau
Conditions
(from sponsor)
Tuberculosis, Mycobacterium Tuberculosis
Related terms Latent Tuberculosis, Tuberculosis
Enrollment 190 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov