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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01192256
Other study ID # 09/WMW01/28
Secondary ID WS763986
Status Completed
Phase
First received
Last updated
Start date March 2010
Est. completion date March 15, 2021

Study information

Verified date August 2022
Source Hywel Dda Health Board
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A large project consisting of: a) an observational trial where smoking status is recorded on 1400 consecutive people newly diagnosed with lung cancer. Smoking status is biologically validated with exhaled carbon monoxide (eCO) levels every 3 months. Survival, cancer progression and treatment complications will be recorded and compared in smokers, ex-smokers and never smokers.


Description:

Smoking causes around 85% of lung cancer. Continued smoking after diagnosis probably worsens survival and increases treatment complications but prospective well-designed studies are lacking. This project is an observational cohort study recording outcomes in smokers, never-smokers, and ex-smokers, using exhaled carbon monoxide to validate smoking status when they attend for further lung cancer clinics. This project is unique, as every patient with a clinical diagnosis of lung cancer will have their smoking status biologically validated by a quick and easy test, and those enrolled in the smoking cessation treatments or not will also complete a generic quality of life questionnaire at regular intervals. These appointments will coincide with other hospital appointments wherever possible, and survival status will reported up to 24 months after enrolment.


Recruitment information / eligibility

Status Completed
Enrollment 2400
Est. completion date March 15, 2021
Est. primary completion date March 15, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - clinical diagnosis of lung cancer Exclusion Criteria: - refusal Consent - inability to provide exhaled CO - active psychiatric illness or substance misuse - concurrent malignancies of another type other than non-melanoma skin cancer - unable to travel for sessions with smoking cessation counsellor and / or outpatient visits from outset - WHO performance status 4 - Life expectancy less than 6 weeks.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Llandough Hospital, Cardiff and Vale University Health Board Cardiff Wales
United Kingdom Hywel Dda Health Board Llanelli Wales

Sponsors (2)

Lead Sponsor Collaborator
Dr Keir Lewis Cardiff and Vale University Health Board

Country where clinical trial is conducted

United Kingdom, 

References & Publications (1)

Gemine RE, Ghosal R, Collier G, Parry D, Campbell I, Davies G, Davies K, Lewis KE; LungCast Investigators. Longitudinal study to assess impact of smoking at diagnosis and quitting on 1-year survival for people with non-small cell lung cancer. Lung Cancer. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Median and 2-year survival rates in confirmed smokers versus non- smokers newly diagnosed with lung cancer. 24 months
Secondary Median survival and 2-year survival rates by smoking status for early (Stage I/II NSCLC) versus those with advanced (Stage III/IV) NSCLC. 24 months
Secondary Number of treatment complications in smokers versus non-smokers (frequency surgical wound complications, radiotherapy induced pneumonitis and median total radiation (Gy) dose; frequency and duration of neutropenic sepses 2 years
Secondary Point prevalence of smoking at 0, 3, 6 12, 24 months 2 years
Secondary Comparison of changes in health related quality of life (EQ5D) in smokers versus non-smokers 2 years
Secondary Accrual and attendance rates of lung cancer patients attending a hospital smoking cessation service 2 years
Secondary Estimate of cost per quality adjusted life year gained by smoking cessation advice in both quit strategies for smokers 2 years
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