RoCCPORT
Research type
Research Study
Full title
A Prospective Cohort Study of Patients with Refractory or Unexplained Chronic Cough measuring Cough Variability and Burden on Patients’ Lives
IRAS ID
357290
Contact name
Amardeep Heer
Contact email
Sponsor organisation
GlaxoSmithKline Research and Development Limited
Duration of Study in the UK
1 years, 0 months, 24 days
Research summary
This study is a multinational, multi-center, observational, prospective, cohort study of patients with RCC/UCC and patients without RCC/UCC using primary data collection. Each patient will participate in the study for a 4-week period (29 days), where they will be asked to complete ePRO questionnaires at specific timepoints and wear a cough monitoring device (smartwatch). No treatment will be provided as a result of participating in this study. Investigators will prescribe treatments based on usual clinical practice. A saliva sample will be collected in RCC/UCC patients that have consented to the optional genetic research.
REC name
South Central - Hampshire A Research Ethics Committee
REC reference
25/SC/0306
Date of REC Opinion
14 Oct 2025
REC opinion
Further Information Favourable Opinion