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A Study of Cesium-131 Brachytherapy Following Sub-Lobar Resection for Early Stage Non Small Cell Lung Cancer

I

IsoRay

Status

Withdrawn

Conditions

Non Small Cell Lung Cancer
NSCLC

Treatments

Radiation: Cesium-131 Brachytherapy Seed

Study type

Observational

Funder types

Industry

Identifiers

NCT01237171
Cs131-Lung001

Details and patient eligibility

About

For patients diagnosed with early (Stage I) non-small cell lung cancer, a lobe of lung is usually removed at surgery to treat the cancer. For some patients, the removal of a lobe of lung may leave too little lung behind for easy breathing. For some of these patients, it may be possible to perform a smaller-scale surgery ("sub-lobar resection") and place a radioactive implant behind to prevent the cancer from growing back. This study will see how these patients do in terms of controlling their disease treated with a radioactive implant called Cesium-131.

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients must have suspicious lung nodule for clinical stage I/recurrent non-small cell Lung Cancer
  2. Mass Tumor size < 7 cm
  3. Patient must have a CT scan of the chest with upper abdomen within 90 days prior to date of pre-registration.
  4. Patient must have ECOG/Zubrod performance status 0,1, or 2.

Exclusion criteria

  1. Patient has already received high dose radiation to the area
  2. Cancerous nodule is very close to the esophagus or spinal cord, thereby increasing the risk of radiation treatment
  3. Pregnancy or unwillingness to practice a form of birth control (i.e. abstinence, oral contraceptives, etc.)

Trial design

0 participants in 1 patient group

Sub-lobar resection with Cesium-131
Description:
All enrolled patients will undergo sub-lobar resection and brachytherapy implant with Cesium-131 in an effort to study and quantify recurrence/control patterns.
Treatment:
Radiation: Cesium-131 Brachytherapy Seed

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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