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NCT01188486 · ClinicalTrials.gov registry record · NA

Pulmonary Interstitial Lymphography in Early Stage Lung Cancer

A NA study, sponsored by Stanford University.

Terminated
Registry status
NA
Development phase
12
Enrollment target

NCT01188486: Clinical Trial NA study, sponsored by Stanford University.

NCT01188486 is a NA study that was terminated before completion, run by Stanford University. The registered enrollment target is 12 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01188486, a NA study, was terminated before completion, sponsored by Stanford University.

TERMINATED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

The stereotactic body radiation therapy (SBRT) procedure is an emerging alternative to the standard treatment for early stage non-small cell lung cancer (NSCLC), typically lobectomy with lymphadenectomy. This procedure (lobectomy) does not fulfill the medical need as many patients are poor operative candidates or decline surgery. This study assesses the feasibility of stereotactic body radiation therapy (SBRT) as a tool to produce therapeutically useful computed tomography (CT) scans, using standard water-soluble iodinated compounds as the contrast agents.

Interventions

  • RADIATION Stereotactic Body Radiation Therapy (SBRT)
  • RADIATION Computed Tomography (CT)
  • DEVICE Cyberknife
  • DEVICE Trilogy
  • DEVICE True Beam

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2010-08
Est. Completion 2017-04-30
Phase NA
Stanford University

1,744 total trials

Why NCT01188486 stopped before completion

NCT01188486 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 5 interventions - of which Stereotactic Body Radiation Therapy (SBRT) is the first listed.

NCT01188486 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01188486 about?

NCT01188486 is a clinical study titled "Pulmonary Interstitial Lymphography in Early Stage Lung Cancer". The stereotactic body radiation therapy (SBRT) procedure is an emerging alternative to the standard treatment for early stage non-small cell lung cancer (NSCLC), typically lobectomy with lymphadenectomy. This procedure (lobectomy) does not fulfill the medical need as many patients are poor operative...

What is the current status of trial NCT01188486?

This trial is currently terminated. It is a NA study. The enrollment target is 12 participants. The study started on 2010-08. Estimated completion is 2017-04-30.

What interventions are being tested in trial NCT01188486?

The interventions under investigation include: Stereotactic Body Radiation Therapy (SBRT) (RADIATION), Computed Tomography (CT) (RADIATION), Cyberknife (DEVICE), Trilogy (DEVICE), True Beam (DEVICE).

Who is sponsoring clinical trial NCT01188486?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01188486's enrollment target sits among peer trials

12 1913th of 2000 higher than 74 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 NCT01188486, the US trial registry maintained by the National Library of Medicine. NCT01188486 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.