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
Discontinued
Discontinued
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
Observational study model:
Case-Control
Primary completion date:
Not applicable
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
Discontinued
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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