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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 Oct 22, 2026, 11:56 PM 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

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

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
Dec 2008 (Type not available)
Primary completion
Mar 2013 (Actual)
Completion
Mar 2013 (Actual)
Last update posted
Jul 14, 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 14, 2020 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00840749 live on ClinicalTrials.gov.

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