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Salford Lung Study

Population Size

Not reported

Years

2012 - 2016

Associated BioSamples

None/not available

Geographic coverage

United Kingdom

England

...see more

Lead time

2-6 months

Summary

Anonymized individual participant data from the Salford Lung Study, annotated CRF, protocol, reporting and analysis plan, dataset specification, associated raw dataset, analysis-ready dataset, and clinical study report are available for research proposals

Documentation

SLS Asthma - Primary Effectiveness Analysis (PEA) - This population is defined as all ITT subjects (all randomised subjects who receive at least one prescription of study medication [e.g. FF/VI or Usual Care]) who have an ACT total score of < 20 at baseline (Day 0). This population will be based on the treatment to which the subject was randomised.

SLS COPD - Primary Effectiveness Analysis (PEA) - This population comprised all ITT subjects (all randomised subjects who received at least one prescription for study medication [e.g. FF/VI or usual care] who had at least one moderate/severe exacerbation in the year prior to Visit 2 (randomisation), as recorded on the eCRF.

Dataset type
Health and disease
Dataset sub-type
Not applicable

Keywords

BREATHE, Asthma Control, COPD Exacerbations, Pragmatic Trial

Provenance

Purpose of dataset collection
Study
Source of data extraction
EPR
Collection source setting
Other
Image contrast
Not stated
Biological sample availability
None/not available

Details

Publishing frequency
Static
Version
1.0.0
Modified

08/10/2024

Distribution release date

04/12/2016

Citation Requirements
GSK

Coverage

Start date

13/03/2012

End date

04/12/2016

Time lag
Not applicable
Geographic coverage
United Kingdom, England, North West, Salford, Manchester
Minimum age range
18
Maximum age range
91

Accessibility

Language
en
Controlled vocabulary
LOCAL
Format
SAS Dataset (.sas7bdat)

Data Access Request

Dataset pipeline status
Not available
Access rights
www.clinicalstudydatarequest.com, https://vivli.org
Time to dataset access
2-6 months
Access method category
Direct access
Access service description
Following receipt of a signed Data Sharing Agreement (DSA), Researchers are provided access to anonymised patient-level data and supporting documentation in a secure data access system, known as the SAS Clinical Trial Data Transparency (CTDT) system.
Data use limitation
General research use
Data Controller
SHARE (GSK data sharing team)
Data Processor
GSK Biostatistics (Respiratory)

Dataset Types: Health and disease


Collection Sources: Other