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NCT01700257 · ClinicalTrials.gov registry record · NA

Lung Cancer Screening Study With Low-dose CT Scan and Blood Biomarker

A NA study, sponsored by National Jewish Health.

Completed
Registry status
NA
Development phase
1,361
Enrollment target

NCT01700257: Completed NA study, sponsored by National Jewish Health.

NCT01700257 is a NA study that has completed, run by National Jewish Health. The registered enrollment target is 1,361 participants, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01700257, a NA study, has completed, sponsored by National Jewish Health.

COMPLETED
Registry status
NA
Development phase
1,361 participants
Enrollment target

Study Summary

Lung cancer is the number one cancer killer in the USA. Early stage lung cancer is asymptomatic. Most patients with lung cancer are usually symptomatic at diagnosis and already have advanced stage disease. Low dose CT screening (LDCT) for high risk individuals has recently been shown to decrease lung cancer mortality by 20%. However, 4 out of 5 lung cancer deaths are not prevented with LDCT screening alone.

Primary Outcome

Assess the number of lung cancers detected with CT alone vs. with both Early CDT-Lung test and CT scan. Compare positive CT results with positive/negative Early CDT Lung test results and assess ability of the combination to detect earlier stage lung cancer.

Interventions

  • RADIATION CT scan & Early CDT Lung test
  • OTHER CT scan & Early CDT Lung test

Trial Details

FieldValue
Enrollment Target 1,361 participants
Start Date 2012-05
Est. Completion 2020-12-07
Phase NA
National Jewish Health

83 total trials

What the finished NCT01700257 record still lists

NCT01700257 is an interventional study that assigns participants to a tested intervention. Its 1,361 participants enrollment target places it among the larger protocols in the corpus, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which CT scan & Early CDT Lung test is the first listed.

NCT01700257 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01700257 about?

NCT01700257 is a clinical study titled "Lung Cancer Screening Study With Low-dose CT Scan and Blood Biomarker". Lung cancer is the number one cancer killer in the USA. Early stage lung cancer is asymptomatic. Most patients with lung cancer are usually symptomatic at diagnosis and already have advanced stage disease. Low dose CT screening (LDCT) for high risk individuals has recently been shown to decrease lun...

What is the current status of trial NCT01700257?

This trial is currently completed. It is a NA study. The enrollment target is 1,361 participants. The study started on 2012-05. Estimated completion is 2020-12-07.

What interventions are being tested in trial NCT01700257?

The interventions under investigation include: CT scan & Early CDT Lung test (RADIATION), CT scan & Early CDT Lung test (OTHER).

Who is sponsoring clinical trial NCT01700257?

This trial is sponsored by National Jewish Health, which has 83 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01700257's enrollment target sits among peer trials

1,361 73rd of 2000 higher than 1,928 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01700257, the US trial registry maintained by the National Library of Medicine. NCT01700257 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.