Ignite Creation Date:
2024-05-05 @ 10:00 AM
Last Modification Date:
2024-10-26 @ 9:05 AM
Study NCT ID:
NCT00006382
Status:
COMPLETED
Last Update Posted:
2015-05-05
First Post:
2000-10-04
Brief Title:
Lung Screening Study
Sponsor:
National Cancer Institute NCI
Organization:
National Cancer Institute NCI
Study Overview
Official Title:
Lung Screening Study
Status:
COMPLETED
Status Verified Date:
2010-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
RATIONALE New imaging procedures such as spiral CT may improve the ability to detect lung cancer in patients who are at high risk for the disease
PURPOSE Randomized clinical trial to compare the effectiveness of a spiral CT scan with that of a chest x-ray in detecting lung cancer in patients who are at high risk for the disease
PURPOSE Randomized clinical trial to compare the effectiveness of a spiral CT scan with that of a chest x-ray in detecting lung cancer in patients who are at high risk for the disease
Detailed Description:
OBJECTIVES I Compare the efficacy of screening spiral CT scan and screening chest x-ray in detecting lung cancer in current or former smokers at high risk for lung cancer
OUTLINE This is a randomized multicenter study of lung cancer screening Patients are randomized to one of two screening arms Arm I Patients undergo one spiral CT scan Arm II Patients undergo one chest x-ray Patients and their primary care physicians are notified of test results within 3 weeks of the exam
PROJECTED ACCRUAL A total of 3000 participants 1500 per screening arm will be accrued for this study at six screening centers 500 per center by October 31 2000
OUTLINE This is a randomized multicenter study of lung cancer screening Patients are randomized to one of two screening arms Arm I Patients undergo one spiral CT scan Arm II Patients undergo one chest x-ray Patients and their primary care physicians are notified of test results within 3 weeks of the exam
PROJECTED ACCRUAL A total of 3000 participants 1500 per screening arm will be accrued for this study at six screening centers 500 per center by October 31 2000
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| NCI-P00-0171 | None | None | None |
| NCI-LUNG | None | None | None |