- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00119470
EUS-FNA in the Pre-Operative Evaluation of Patients With Lung Cancer
December 19, 2007 updated by: University Hospital, Ghent
EUS-FNA in the Pre-Operative Evaluation of Patients With Lung Cancer: A Randomized Trial
This trial examines the role of EUS-FNA (Oesophageal Endoscopic Ultrasound with Fine Needle Aspiration) as an endoscopic technique for the mediastinal staging of patients with lung cancer.
Patients will be randomized to either conventional surgical technique or EUS-FNA.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment
40
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ghent, Belgium, 9000
- University Hospital Ghent
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients with histological or cytological proof of non small cell lung cancer (NSCLC) or with a high clinical suspicion for lung cancer (but without pathologically confirmed diagnosis from the bronchoscopy or CT guided transthoracal biopsies) in whom the next step is normally a diagnostic or therapeutic surgical intervention
- no distant metastases after routine clinical work up (PET is optional, not mandatory)
- provision of a written informed consent
- recent CT-scan of the thorax (<28 days before randomization date)
- age 18 years or older
- clinically fit for surgery
Exclusion Criteria:
- proof of small cell lung cancer (SCLC) with CWU (bronchoscopy or CT guided transthoracal punction)
- stage IV NSCLC
- patients with a solitary pulmonary nodule (thus without enlarged mediastinal lymph nodes on CT and without mediastinal PET hot spots) : these do not require further mediastinal investigation
- former therapy (chemotherapy or radiotherapy or surgery) for lung cancer
- other concomitant malignancies
- reasons for which the patient is unable to swallow the EUS-instrument (e.g. zenker diverticulum, unexplained esophageal stenosis)
- uncorrected coagulopathy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Percentage of surgical interventions avoided
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Secondary Outcome Measures
Outcome Measure |
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Accuracy of EUS-FNA for mediastinal staging of lung cancer
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kurt Tournoy, MD, University Hospital, Ghent
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2005
Study Completion (Actual)
February 1, 2007
Study Registration Dates
First Submitted
July 1, 2005
First Submitted That Met QC Criteria
July 2, 2005
First Posted (Estimate)
July 13, 2005
Study Record Updates
Last Update Posted (Estimate)
December 28, 2007
Last Update Submitted That Met QC Criteria
December 19, 2007
Last Verified
December 1, 2007
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2004/276
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Bin ChengCompleted
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National Cancer Center, KoreaCompleted
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AdventHealthUniversity of Alabama at BirminghamCompletedPancreatic CancerUnited States
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Johns Hopkins UniversityBoston Scientific CorporationCompletedPancreatic Solid Lesions | Pancreatic MassUnited States
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Mauna Kea TechnologiesUnknownPancreatic Neoplasms | Pancreatic Cancer | Lymphadenopathy | Pancreatic Cyst | Pancreatic Islet Cell Tumors | Pancreatic Adenoma | Lymph NodeFrance
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Region SkaneTerminatedGastrointestinal NeoplasmsSweden