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Clinical trialNCT00840749TerminatedInterventional

Randomized Study to Compare CyberKnife to Surgical Resection In Stage I Non-small Cell Lung Cancer

SponsorAccuray IncorporatedEnrollment36Non-small Cell Lung Cancer
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Lung cancer remains the most frequent cause of cancer death in both men and women in the world. Surgical resection using lobectomy with mediastinal lymph node dissection or sampling has been a standard of care for operable early stage NSCLC. Several studies have reported high local control and survival using SBRT in stage I NSCLC patients. SBRT is now an accepted treatment for medically inoperable patients with stage I NSCLC and patients with operable stage I lung cancer are entered on clinical protocols. The purpose of this study is to conduct a phase III randomized study to compare CyberKnife SBRT with surgery, the current standard of care for stage I operable NSCLC.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

19 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

China
  • Ruikang Hospital

    Nanning, Guangxi, China

  • Tianjin Cancer Institute and Hospital

    Hexi Linchang, Tianjin Municipality, China

France
  • Centre Oscar Lambret

    Lille, France

  • Centre Antoine Lacassagne

    Nice, France

Taiwan
  • Cyberknife Center of Wanfang Medical Hospital

    Taipei, Taiwan

United States
  • Community Regional Medical Center

    Fresno, California, United States

  • Penrose Cancer Center

    Colorado Springs, Colorado, United States

  • Denver Cyberknife

    Lone Tree, Colorado, United States

  • Jupiter Medical Center

    Jupiter, Florida, United States

  • Advocate Christ Medical Center

    Oak Lawn, Illinois, United States

  • Parkview Cancer Center

    Fort Wayne, Indiana, United States

  • Central Baptist Hospital

    Lexington, Kentucky, United States

  • St. Joseph Mercy Hospital

    Ann Arbor, Michigan, United States

  • St. Mary'S of Michigan

    Saginaw, Michigan, United States

  • St. Mary'S Duluth Clinic Health System

    Duluth, Minnesota, United States

  • Saint Louis University

    St Louis, Missouri, United States

  • St. Mary'S

    Reno, Nevada, United States

  • St. Luke'S Episcopal Hospital

    Houston, Texas, United States

  • U.T. M.D. Anderson Cancer Center

    Houston, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Dec 2008
Primary completion
31 Mar 2013
Completion
31 Mar 2013
Last update posted
14 Jul 2020
Registered enrollment
36
Registry id
NCT00840749

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.