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Non-risk Based Lang Cancer Screening With a One-off LDCT

Non-risk Based Lung Cancer Screening With One-time Low-dose Computed Tomography: a Prospective Cohort Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04938804
Enrollment
11000
Registered
2021-06-24
Start date
2015-12-12
Completion date
2026-12-01
Last updated
2024-01-09

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

Conditions

Lung Cancer

Keywords

Screening

Brief summary

Guangzhou Lung-Care Project is a single-arm, prospective cohort study using one-time low-dose computed tomography for the early detection of LC, recruiting residents aged 40-74 years from four communities in Guangzhou between 2015 and 2021.The primary outcome was LC detection rate in eligible participants without restrictions based on high-risk factors and the proportion of stage I LC cases, and to investigate the various factors associated with the development of LC.

Detailed description

Guangzhou Lung-Care Project is a single-arm, prospective cohort study using one-time low-dose computed tomography for the early detection of LC, recruiting residents aged 40-74 years from four communities in Guangzhou between 2015 and 2021. Follow-up for post-screening management and survival was recorded. The primary outcome was LC detection rate in eligible participants without restrictions based on high-risk factors and the proportion of stage I LC cases, and to investigate the various factors associated with the development of LC. Additionally, we compared the detection rates of LC and the proportion of stage I LC cases between high-risk and non-high-risk groups according to the National Comprehensive Cancer Network (NCCN) guidelines and Chinese guideline.

Interventions

The Low-dose computed tomography is conducted according to the guideline suggested by American College of Radiology.

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 74 Years
Healthy volunteers
Yes

Inclusion criteria

* Minimum age of 40 years among the residents in Guangzhou

Exclusion criteria

* Persons who had a diagnosis or treatment related to LC within the past 5 years, had undergone chest CT within the past year, or had significant cancer-related symptoms (e.g., hemoptysis, dyspnea, inability to climb two flights of stairs).

Design outcomes

Primary

MeasureTime frameDescription
The detection rate of lung cancer11 yearsLung cancer detection rate in eligible participants without restrictions based on high-risk factors and the proportion of stage I LC cases.
To investigate the various factors associated with the development of lung cancer11 yearsTo investigate the various factors associated with the development of lung cancer

Secondary

MeasureTime frameDescription
Detection rates of lung cancer and the proportion of stage I lung cancer cases between high-risk and non-high-risk groups11 yearsThe detection rate of lung cancer among people with high-risk and non-high-riskfactors
Cost-effectiveness ratio (costs of examinations, diagnoses, and treatments)11 years

Countries

China

Contacts

Primary ContactWenhua Liang, MD
liangwh1987@163.com+86-02-83062808

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026