A study to identify and characterise bacteria causing chronic cough among children in United Kingdom
Trial overview
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
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
- 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.
- A male or female child between, and including, six to 72 months of age at the time of enrolment.
- Written informed consent obtained from the parent(s)/ legally acceptable representative of the subject.
- No antibiotic therapy within four weeks prior to the visit.
- No cystic fibrosis or known major immunodeficiency such as agammaglobulinaemia, T cell deficiency or Human Immunodeficiency Virus / Acquired Immune Deficiency Syndrome.
- No documented evidence or suspicion of gastroesophageal reflux disease.
- No evidence of an upper viral respiratory infection four weeks prior to the visit. In addition, all subjects regarded as ‘cases’ must satisfy all the following criteria at study entry:
- Persistent cough greater than eight weeks.
- No response to five-day prednisolone treatment.
- Chest X-ray showing no evidence of a lobar pneumonia or gross structural abnormality. In addition, all subjects regarded as ‘controls’ must satisfy the following criteria at study entry:
- No respiratory symptoms four weeks prior to the visit.
- No documented evidence or suspicion of lung disease upon physical examination.
Subjects who the investigator believes that parent(s)/ legally acceptable representative can and will comply with the requirements of the protocol.
- Use of any investigational or non-registered product within 30 days prior to study procedures, or planned use during the study period.
- Any confirmed or suspected immunosuppressive or immunodeficient condition, based on medical history and physical examination.
- Child in care.
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.
Trial location(s)
Study documents
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Plain language summaries
Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.