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Spots Global Cancer Trial Database for National Lung Screening Trial (NLST) Screening

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Trial Identification

Brief Title: National Lung Screening Trial (NLST) Screening

Official Title: National Lung Screening Trial A Randomized Trial Comparing Low-dose Helical CT With Chest Xray for Lung Cancer

Study ID: NCT00047385

Conditions

Lung Cancer

Study Description

Brief Summary: RATIONALE: Effective screening tests should help doctors detect lung cancer early and plan curative treatment. It is not yet known whether low-dose helical computed tomography (LDCT) screening is more effective than chest radiography (CXR) screening in reducing death from lung cancer. PURPOSE: Randomized clinical trial to compare the effectiveness of LDCT scan with that of CXR in screening individuals who are at high risk for developing lung cancer.

Detailed Description: OBJECTIVES: * Compare whether screening with low-dose helical CT scan vs chest x-ray reduces lung cancer-specific mortality in participants who are at high risk for developing lung cancer. OUTLINE: NLST participants were randomized to either low-dose helical CT or chest x-ray in equal proportions. A total of 53,454 participants were enrolled (26,722 in low-dose CT and 26,732 in chest radiography) at 33 screening centers across the United States. Screening was offered three times (at baseline and two annual follow-up examinations). The primary endpoint of the study was lung cancer mortality. The study arms were compared with regard to overall mortality, lung cancer incidence, and screening-related complications. All low-dose scanners and chest x-ray machines were certified for use and met NLST protocol requirements and American College of Radiology guidelines. Low-dose CT acquisitions and chest radiographs were interpreted by trained radiologists. Participants and their health care provider were informed of study examination results. Participants with abnormalities suspicious for lung cancer were contacted for information regarding diagnostic evaluation. Medical records were collected on diagnostic evaluation, medical complications, and initial treatment. Participants were then contacted at least annually by mail or telephone. The National Lung Screening Trial (NLST) represents the union of two NCI-sponsored efforts, the NCI Lung Screening Study and the American College of Radiology Imaging Network (ACRIN).

Eligibility

Minimum Age: 55 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

Univeristy of California, San Diego, La Jolla, California, United States

Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, California, United States

University of Colorado Denver, Denver, Colorado, United States

Georgetown University Medical Center, Washington, District of Columbia, United States

Mayo Clinic, Jacksonville, Florida, United States

H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, United States

Emory University School of Medicine, Atlanta, Georgia, United States

Pacific Health Research & Education Institute, Honolulu, Hawaii, United States

Northwestern University, Chicago, Illinois, United States

University of Iowa, Iowa City, Iowa, United States

Jewish Hopsital Heart and Lung Institute, Louisville, Kentucky, United States

Ochsner Medical Foundation Hospital, New Orleans, Louisiana, United States

Johns Hopkins University, Baltimore, Maryland, United States

Brigham and Women's Hospital, Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, United States

Henry Ford Health System, Detroit, Michigan, United States

University of Minnesota School of Public Health, Minneapolis, Minnesota, United States

Mayo Clinic Cancer Center, Rochester, Minnesota, United States

Washington University School of Medicine, St. Louis, Missouri, United States

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, United States

Cancer Institute of New Jersey at Hamilton, Hamilton, New Jersey, United States

Wake Forest University, Winston-Salem, North Carolina, United States

St Elizabeth Health Center, Youngstown, Ohio, United States

University of Pennsylvania Medical Center, Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

Brown University, Rhode Island Hospital, Providence, Rhode Island, United States

Medical University of South Carolina, Charleston, South Carolina, United States

Vanderbilt University, Nashville, Tennessee, United States

University of Texas - MD Anderson Cancer Center, Houston, Texas, United States

University of Utah Health Sciences Center, Salt Lake City, Utah, United States

Marshfield Clinic Research Foundation, Marshfield, Wisconsin, United States

Contact Details

Name: Christine D. Berg, MD

Affiliation: NCI - Early Detection Research Group

Role: STUDY_DIRECTOR

Name: Denise R. Aberle, MD

Affiliation: Jonsson Comprehensive Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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