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Vessel Interruption Order for Lung Cancer (CTC-01 Trial)
N/A
Waitlist Available
Led By Massimo Conti, MD
Research Sponsored by Laval University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Clinical stage tumor-1 to 3, clinical stage node-0, clinical stage metastasis-0 (except clinical stage tumor-3 for chest wall, pericardium or phrenic nerve invasion)
NSCLC with preoperative pathological evidence
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within 96 hours after surgery
Awards & highlights
CTC-01 Trial Summary
This trial will help determine if the order in which a surgeon interrupts the vessels leading to a tumor affects the density of cancer cells in the area.
Who is the study for?
This trial is for adults with non-small cell lung cancer (NSCLC) who have a certain type of tumor visible on a CT scan and are in the early stages of the disease. They must be candidates for minimally invasive lung surgery but haven't had thoracic surgery on the same side before, nor can they have received recent cancer treatment or have another active cancer.Check my eligibility
What is being tested?
The study is testing whether interrupting blood flow through veins before other surgical steps, or arteries before veins, affects circulating tumor cells during lung cancer surgery. The goal is to see if changing this sequence impacts how many tumor cells spread from the lungs into the blood.See study design
What are the potential side effects?
Since this trial focuses on surgical technique rather than medication, typical drug-related side effects aren't expected. However, risks may include those associated with any surgical procedure such as bleeding, infection, and complications related to anesthesia.
CTC-01 Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My cancer is in an early stage and has not spread to lymph nodes or other parts of the body.
Select...
My lung cancer was confirmed by a biopsy before surgery.
Select...
I had a minimally invasive lung surgery.
CTC-01 Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within 96 hours after surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within 96 hours after surgery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Changes in CTC clusters density
Changes in CTC density
Secondary outcome measures
Disease free survival
Overall survival
CTC-01 Trial Design
2Treatment groups
Active Control
Group I: Arteries before veinActive Control1 Intervention
Lobar arteries (+/- bronchus and inter-lobar fissures) are interrupted before tumor-draining pulmonary vein.
Group II: Vein firstActive Control1 Intervention
Tumor-draining pulmonary vein is interrupted first and before any surgical manipulation.
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Who is running the clinical trial?
Laval UniversityLead Sponsor
417 Previous Clinical Trials
172,242 Total Patients Enrolled
Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de QuebecOTHER
36 Previous Clinical Trials
9,712 Total Patients Enrolled
Massimo Conti, MDPrincipal InvestigatorCentre de Recherche IUCPQ - Laval University
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have not had a diagnosis based on tissue samples taken before surgery.My first lung surgery was done by opening the chest with rib spreading.I have had chest surgery on the same side before.My cancer has spread to my chest wall or nearby areas.My cancer has spread to at least one lymph node.I am not pregnant and I am 18 years old or older.My lung was stuck to another organ, making initial blood sampling difficult.My cancer is in an early stage and has not spread to lymph nodes or other parts of the body.I have not had a second cancer or any cancer in the past 5 years.You have a specific type of abnormal spot on your CT scan called a pure ground glass nodule.I need additional surgery beyond the removal of a lung lobe.My lung cancer was confirmed by a biopsy before surgery.I had a minimally invasive lung surgery.You have a specific type of nodule in your lungs that shows up on a CT scan.I have received treatment before the main cancer treatment.I have had a type of lung surgery.
Research Study Groups:
This trial has the following groups:- Group 1: Arteries before vein
- Group 2: Vein first
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is this research study recruiting participants at the moment?
"As indicated on clinicaltrials.gov, the current iteration of this medical experiment is not enlisting participants; it was first published on August 31st 2018 and updated most recently on the 22nd of that same month. Fortunately, there are 1898 other trials actively looking for volunteers at present."
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