Randomized Study to Compare CyberKnife to Surgical Resection In Stage I Non-small Cell Lung Cancer
Summary
The lay summary the sponsor registered on ClinicalTrials.gov.
Investigators
The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.
- Jack Roth, M.D.
M.D. Anderson Cancer Center
Principal Investigator
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.
- Ruikang Hospital
Nanning, Guangxi, China
- Tianjin Cancer Institute and Hospital
Hexi Linchang, Tianjin Municipality, China
- Centre Oscar Lambret
Lille, France
- Centre Antoine Lacassagne
Nice, France
- Cyberknife Center of Wanfang Medical Hospital
Taipei, Taiwan
- 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.