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An Observational Study of Predictors and Outcomes of Lung Cancer in Never-smokers in the UK

An Observational Study of Predictors and Outcomes of Lung Cancer in Never-smokers in the UK

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06575439
Acronym
OLIVE
Enrollment
225
Registered
2024-08-28
Start date
2024-09-17
Completion date
2029-09-30
Last updated
2024-12-12

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

Conditions

Lung Cancer

Brief summary

The goal of this observational study is to improve the early detection of lung cancer in adults who have smoked less than 100 tobacco cigarettes (never-smokers) in the United Kingdom. The main questions it aims to answer are: * To describe characteristics such as demographics, co-morbidities and environmental exposures * To describe participant pathways including presentation mode and symptoms to understand if earlier diagnosis would be possible * To describe participant outcomes such as cancer stage, treatment and mortality * To quantitatively or qualitatively measure modifiable and non-modifiable factors that may be associated with LCINS including environmental measures, blood tests and genomic data. Participants will currently have no change to their usual care.

Interventions

None listed

Sponsors

University College London Hospitals
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All adult participants from age of 18 who are diagnosed or treated with primary lung cancer through radiology or histology at any participating study site

Exclusion criteria

* Participants who have ever smoked cigarettes or tobacco will be excluded; this is defined as: * More than 100 cigarettes or 75g tobacco in their lifetime * Those who have received a prescription for nicotine replacement therapy * For prospective participants, those who cannot consent will be excluded

Design outcomes

Primary

MeasureTime frameDescription
Demographics, comorbidities and environmental exposures of participantsComorbidities and environmental exposures at diagnosis (approximately up to 156 weeks prior to diagnosis)From review of electronic health records
Participant pathways including presentation mode and symptomsPresentation mode and symptoms at time of diagnosis (approximately up to 52 weeks prior to diagnosis)From review of electronic health records

Secondary

MeasureTime frameDescription
Participant outcomes such as cancer stage, treatment, mortalityCancer stage at time of diagnosis, treatment and mortality through study completion (likely 5 years)From review of electronic health records
Measurement of modifiable and non-modifiable factors associated with LCINSThrough study completion (likely 5 years)To be determined

Countries

United Kingdom

Contacts

Primary ContactNeal Navani, PhD
n.navani@ucl.ac.uk020 7679 2000
Backup ContactSindhu Naidu, MBBS
s.naidu@ucl.ac.uk020 7679 2000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026