UK lung volume reduction trial

UK Lung Volume Reduction: a multicentre observational study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ISRCTN

Registry ID

ISRCTN16371361

Enrollment

300

Registered

2017-01-09

Start date

2016-12-01

Completion date

Unknown

Last updated

2022-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emphysema Respiratory Emphysema

Interventions

Lung volume reduction procedures for emphysema include lung volume reduction surgery, endobronchial valve placement, lung volume reduction coils. This study collects data from people undergoing these

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients aged over 18 with emphysema undergoing a lung volume reduction procedure

Exclusion criteria

Exclusion criteria: Not meeting the inclusion criteria

Design outcomes

Primary

Measure	Time frame
Forced expiratory volume in one second, measured by spirometry at baseline and 3 months post procedure	—

Secondary

Measure	Time frame
1. Walking distance, measured by 6 minute walk test or incremental shuttle walk test, at baseline, 3 and 12 months 2. Health status, measured by COPD assessment test (CAT) score or SGRQ at baseline, 3 and 12 months 3. Residual volume, measured by body plethysmography at baseline, 3 and 12 months	—

Countries

England, United Kingdom, Wales

Contacts

Public ContactSara Buttery

s.buttery@rbht.nhs.uk+44 (0)207 351 8029

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026