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NCT02719847Completed

EBUS TBNA After PET/CT in Diagnosing Patients With Stage I-IIA Non-small Cell Lung Cancer Evaluated for Stereotactic Body Radiation Therapy

Additive Value of EBUS TBNA for Staging Non-Small Cell Lung Cancer in Patients Evaluated for Stereotactic Body Radiation Therapy

Source: ClinicalTrials.gov · Last updated 23 Sept 2025

Brief summary (registry, in English)

This clinical trial studies how well endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) after positron emission tomography/computed tomography (PET/CT) scan works in diagnosing patients with stage I-IIA non-small cell lung cancer evaluated for stereotactic body radiation therapy (SBRT). Performing EBUS-TBNA after PET/CT scan may help doctors learn more about the accuracy and ways to find early stage lung cancer.

Status (registry)
Completed
Study type
Observational
Enrollment
150 (estimated)
First submitted
21 Mar 2016
Start date
18 Mar 2016
Primary completion date
12 Sept 2025
Lead sponsor
M.D. Anderson Cancer Center
Diseases
Lung cancer
NCT number
NCT02719847

What you commit to

  • Study type: Observational
  • Planned participants: 150
  • From 18 Mar 2016 to the primary completion date, 12 Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient has received prior chemotherapy or radiotherapy for this cancer

Other illness

  • Patients already scheduled to receive conventional radiotherapy, chemotherapy, biological therapy, vaccine therapy, or surgery as treatment (except at disease progression)
  • Patients malignancy is consistent with well differentiated neuroendocrine (carcinoid) histology

Other

  • Patients who are planning to undergo treatment in a different institution

Who the study is looking for

  • Patient must be \> 18 years old
  • Patient must have proven or suspected non small cell lung cancer (NSCLC) and be clinical Stage I or IIa, according to the 7th edition staging system of the American Joint Commission on Cancer for lung cancer (T1 or T2a, N0 or N1, M0)
  • Patient must have a PET/CT obtained within 40 days of having the EBUS-TBNA
  • Patient is being considered for SBRT
  • Patient or the patient's legally authorized representative must provide written informed consent prior to registration and any study-related procedures
  • If the patient is a survivor of a prior invasive cancer, all of the following criteria must apply: a) Patient has undergone potentially curative therapy for all prior malignancies b) No evidence of active / recurrent disease within 5 years

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Texas - MD Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.