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Salford Lung Study

Population Size

Not reported
Population Size statistic card

Years

2012 - 2016

Years statistic card

Associated BioSamples

None/not available

Associated BioSamples statistic card

Geographic coverage

United Kingdom

England

...see more

Geographic coverage statistic card

Lead time

2-6 months

Lead time statistic card

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

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

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