Molecular Assessment of Lymph Nodes in Patients With Resected (Stage I to IIIA) Non-small Cell Lung Cancer
Research of Molecular Markers for Diagnosis and/or Prognosis in Lymph Node Metastasis of Resected Non-small Cell Lung Cancer
1 other identifier
observational
150
1 country
5
Brief Summary
This is a prospective study of surgically resected samples and lymph nodes of lung cancer patients. For histopathologically positive lymph nodes from a complete resection, the investigators would like to analyse tumor tissue by allelotyping and comparing these results with those observed in the primary lung tumor to establish a cartography of molecular alteration in resected lung cancer. For non histopathologically positive lymph nodes, the investigators would like to research the presence (or not) of micrometastasis by allele-specific PCR (polymerase chain reaction).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jun 2004
Longer than P75 for all trials
5 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2004
CompletedFirst Submitted
Initial submission to the registry
September 13, 2005
CompletedFirst Posted
Study publicly available on registry
September 21, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2011
CompletedAugust 30, 2011
August 1, 2011
September 13, 2005
August 29, 2011
Conditions
Keywords
Eligibility Criteria
Patients with resectable non-small cell lung cancer (stage I to IIIA), with a complete resection of the tumor and paired lymph nodes
You may qualify if:
- Patients with resectable non-small cell lung cancer (stage I to IIIA), with a complete resection of the tumor and paired lymph nodes.
- Informed consent is required.
You may not qualify if:
- Another cancer
- Chemotherapy before surgical treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (5)
Service de Chirurgie Thoracique, Hôpital Civil
Strasbourg, 67091, France
Service de Pneumologie, Hôpital Lyautey
Strasbourg, 67091, France
Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital de Hautepierre
Strasbourg, 67098, France
Service d'Anatomie Pathologique, Hôpital de Hautepierre
Strasbourg, 67098, France
Service de Pneumologie, Hôpital de Hautepierre
Strasbourg, 67098, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michèle BEAU-FALLER, MD
Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital de Hautepierre
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 13, 2005
First Posted
September 21, 2005
Study Start
June 1, 2004
Study Completion
August 1, 2011
Last Updated
August 30, 2011
Record last verified: 2011-08