We have a specialist cough team are available to work on cough studies and this includes Project Managers, 7 UK based CRAs and 8 US based CRAs.
All members of this specialist team have extensive industry experience and experience of working with VitaloJAKs – a 510(K) FDA approved and CE marked custom-built digital recording device (VitaloJAK, Vitalograph Ltd) and currently the only FDA approved cough monitor for use in clinical trials. Additionally, we have conducted cough challenge studies involving the inhalation of tussive agents/substances such as ATP, Capsaicin, Citric Acid and Distilled Water. These substances were inhaled via a neubulizer, controlled by the KoKo DigiDoser and the number of induced coughs counted.
Illingworth has a unique set-up for specific respiratory studies, engaging with selected commercial ‘super-sites’ in the UK and Europe, giving you access to unprecedented patient numbers to take part in these trials. These ‘super-sites’ have a comprehensive pedigree in respiratory research and are considered experts in this therapeutic area, both in device and drug studies.
Illingworth Research Group has many highly experienced respiratory Project Managers and CRA’s who co-ordinate the submissions required to set up the studies within these sites. Since the UK ‘super-sites’ are commercial units and therefore outside of the National Health Service, they do not require R&D approvals and can, as a result, obtain decisions very rapidly making it an attractive option for sponsors.
- Body boxes
- Various spirometers
- Exercise challenge equipment
- Lung clearance index
- Challenge chambers
- FeNO (nasal/exhaled) plus differential NO
- Vibration resonance imaging
- Exercise testing VO2 max
- Central spirometry over reading
- Doppler USS and 64 slice PET/ CT
- Full endoscopy and bronchoscopy services
- Biomarker laboratory
Please click on the link below for the case study.