Last updated: 11/03/2018 13:54:52

A study to identify and characterise bacteria causing chronic cough among children in United Kingdom

GSK study ID
112956
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Other
Other
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Identification and characterisation of bacteria causing chronic cough among children in the United Kingdom
Trial description: The purpose of this study is to investigate the role of Haemophilus influenzae and other bacteria in causing chronic cough, through a direct comparison of chronic cough cases and healthy controls recruited from paediatric respiratory clinics in the United Kingdom.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:

Occurrence of Haemophilus influenzae, in the absence of co-infection with other bacteria, in the lower airways of cases and controls

Timeframe: 12–15 months from study initiation

Secondary outcomes:

Occurrence of Haemophilus influenzae, regardless of co-infection with other bacteria, in the lower airways of cases and controls

Timeframe: 12–15 months from study initiation

Occurrence of Streptococcus pneumoniae in the lower airways of cases and controls

Timeframe: 12–15 months from study initiation

Occurrence of Haemophilus influenzae in cough swabs and nasopharynx/ oropharynx of cases and controls

Timeframe: 12–15 months from study initiation

Occurrence of Haemophilus influenzae in the lower airways and/or nasopharynx/ oropharynx of cases and controls

Timeframe: 12–15 months from study initiation

Bacterial load of Haemophilus influenzae in the lower airways and nasopharynx/ oropharynx of cases and controls

Timeframe: 12–15 months from study initiation

Occurrence of Haemophilus haemolyticus in the lower airways and nasopharynx/ oropharynx of cases and controls

Timeframe: 12–15 months from study initiation

Antimicrobial resistance of Haemophilus influenzae in lower airways

Timeframe: 12–15 months from study initiation

Occurrence of viral pathogens in the lower airways and nasopharynx of cases and controls

Timeframe: 12–15 months from study initiation

Occurrence of Moraxella catarrhalis in the lower airways of cases and controls

Timeframe: 12-15 months from study initiation

Occurrence of other bacterial pathogens in the lower airways of cases and controls

Timeframe: 12-15 months from study initiation

Occurrence of Streptococcus pneumoniae in cough swabs and nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Occurrence of Moraxella catarrhalis in cough swabs and nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Occurrence of Streptococcus pneumoniae in the lower airways and/or nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Occurrence of other bacterial pathogens in the lower airways and/or nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Bacterial load of Streptococcus pneumoniae in the lower airways and nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Bacterial load of Moraxella catarrhalis in the lower airways and nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Occurrence of serotypes of Haemophilus influenzae in the lower airways and nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Occurrence of serotypes of Streptococcus pneumoniae in the lower airways and nasopharynx/ oropharynx of cases and controls

Timeframe: 12-15 months from study initiation

Antimicrobial resistance of Streptococcus pneumoniae in lower airways

Timeframe: 12-15 months from study initiation

Antimicrobial resistance of Moraxella catarrhalis in lower airways

Timeframe: 12-15 months from study initiation

Interventions:
  • Procedure/surgery: Cough swab
  • Procedure/surgery: Oropharyngeal swab
  • Procedure/surgery: Nasopharyngeal swabs
  • Procedure/surgery: Blood sample
  • Procedure/surgery: Bronchoscopy/ bronchoalveolar lavage samples
  • Other: Data collection
  • Enrollment:
    19
    Primary completion date:
    Not applicable
    Observational study model:
    Case-Control
    Time perspective:
    Prospective
    Clinical publications:
    Not applicable
    Medical condition
    Infections, Respiratory Tract
    Product
    GSK2647154A
    Collaborators
    Not applicable
    Study date(s)
    May 2012 to February 2013
    Type
    Observational
    Phase
    Not applicable

    Participation criteria

    Sex
    Female & Male
    Age
    6 - 72 months
    Accepts healthy volunteers
    No
    • Subjects who the investigator believes that parent(s)/ legally acceptable representative can and will comply with the requirements of the protocol.
    • A male or female child between, and including, six to 72 months of age at the time of enrolment.
    • Concurrently participating in another study, at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product.
    • Use of any investigational or non-registered product within 30 days prior to study procedures, or planned use during the study period.

    Trial location(s)

    Location
    Status
    Contact us
    Contact us
    Location
    GSK Investigational Site
    Sheffield, United Kingdom, S10 2TH
    Status
    Study Complete
    Location
    GSK Investigational Site
    Bristol, United Kingdom, BS2 8AE
    Status
    Terminated/Withdrawn
    Location
    GSK Investigational Site
    Belfast, United Kingdom, BT12 6BE
    Status
    Terminated/Withdrawn

    Study documents

    Scientific result summary
    Available language(s): English

    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Refer to study documents

    Recruitment status
    Other
    Actual primary completion date
    Not applicable
    Actual study completion date
    2013-10-02

    Plain language summaries

    Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.

    Additional information about the trial

    Not applicable
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