Non-small Cell Lung Cancer Clinical Trial
Official title:
Comparison of Diagnostic and Therapeutic Efficacy of Endobronchial/Endoesophageal Ultrasound and Transcervical Extended Mediastinal Lymphadenectomy in Non-Small-Cell Lung Cancer. A Randomised Controlled Trial
NCT number | NCT03188562 |
Other study ID # | 02/2014 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 1, 2011 |
Est. completion date | December 1, 2017 |
Verified date | May 2019 |
Source | Pulmonary Hospital Zakopane |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of the study is prospective comparison of diagnostical and therapeutical efficiency
between different methods of mediastinal lymph node preoperative staging in Non-Small-Cell
Lung Cancer (NSCLC).
Two hundred patients with histologically/cytologically confirmed clinical stage primary
I-IIIA NSCLC will be included. The patients must be fit enough to undergo at least pulmonary
lobectomy. Computer Tomography (CT) and Positron Emission Tomography (PET/CT) will be
performed in all patients. Subsequently, the patients without evidence of dissemination will
be randomized to transbronchial and transesophageal endoscopic ultrasound-guided needle
aspiration ( EBUS-TBNA, EUS-NA) or Transcervical Extended Mediastinal Lymphadenectomy
(TEMLA). The patients with N3 will be referred to definitive oncological treatment, the
patients with N2 metastases will be referred to neoadjuvant treatment and the patients
without N2/3 metastases will be operated on. The operative procedure will include at least
lobectomy with complete lymphadenectomy, with open or video-assisted (VATS) technique. The
patients undergoing sublobar resection will be excluded from this study. Final analysis will
include comparison of the diagnostic yield and 5-year survival between the EBUS/EUS and the
TEMLA arms.
Status | Completed |
Enrollment | 200 |
Est. completion date | December 1, 2017 |
Est. primary completion date | December 1, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion Criteria: - patients with histologically or cytologically proven clinical stage I-IIIA NSCLC - no medical contraindication to operation with at least pulmonary lobectomy - adequate cardiac and pulmonary function Exclusion Criteria: - previous cancer treatment history |
Country | Name | City | State |
---|---|---|---|
Poland | Pulmonary Hospital | Zakopane |
Lead Sponsor | Collaborator |
---|---|
Pulmonary Hospital Zakopane |
Poland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | comparison of the diagnostic yield of EBUS/EUS and TEMLA | after radical surgical treatment (lobectomy or pneumonectomy with lymphadenectomy) | 2 weeks after the end of surgery | |
Secondary | 5-year survival between the EBUS/EUS and the TEMLA arms | individual or phone contact with each patient | 5-year |
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