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Terminated Not applicable Interventional Results available

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

ClinicalTrials.gov ID: NCT00840749

Public ClinicalTrials.gov record NCT00840749. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 24, 2026, 3:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

International Randomized Study to Compare CyberKnife® Stereotactic Radiotherapy With Surgical Resection in Stage I Non-small Cell Lung Cancer

Study identification

NCT ID
NCT00840749
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Accuray Incorporated
Industry
Enrollment
36 participants

Conditions and interventions

Interventions

  • CyberKnife Stereotactic Radiotherapy Radiation
  • Surgery Procedure

Radiation · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2008
Primary completion
Feb 28, 2013
Completion
Feb 28, 2013
Last update posted
Jul 13, 2020

2008 – 2013

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Community Regional Medical Center Fresno California 93721
Penrose Cancer Center Colorado Springs Colorado 80907
Denver CyberKnife Lone Tree Colorado 80124
Jupiter Medical Center Jupiter Florida 33458
Advocate Christ Medical Center Oak Lawn Illinois 60453
Parkview Cancer Center Fort Wayne Indiana 46845
Central Baptist Hospital Lexington Kentucky 40503
St. Joseph Mercy Hospital Ann Arbor Michigan 48106
St. Mary's of Michigan Saginaw Michigan 48601
St. Mary's Duluth Clinic Health System Duluth Minnesota 55805
Saint Louis University St Louis Missouri 63110
St. Mary's Reno Nevada 89503
St. Luke's Episcopal Hospital Houston Texas 77030
U.T. M.D. Anderson Cancer Center Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00840749, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 13, 2020 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00840749 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →