Actively Recruiting
Exploration on the Value of MRD Based on ctDNA Detection in Predicting Recurrence of Resected Non-small Cell Lung Cancer
Led by Shanghai Pulmonary Hospital, Shanghai, China · Updated on 2024-02-21
377
Participants Needed
1
Research Sites
248 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Based on the unique patented MONOD and Methyl Titan methylation sequencing technology on lung cancer tissue and blood samples, a lung cancer MRD monitoring panel is designed. The panel is used to detect molecular residual disease of stage IB-IIIB non-small cell lung cancer patients underwent radical surgery, explore personalized analysis models, and conduct research on recurrence monitoring for non-small cell lung cancer patients.
CONDITIONS
Official Title
Exploration on the Value of MRD Based on ctDNA Detection in Predicting Recurrence of Resected Non-small Cell Lung Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosed with non-small cell lung cancer at clinical stage IB to IIIB
- Able to undergo radical surgical treatment
- Physical condition score (ECOG) of 1 or less
- Expected survival time longer than 24 months
- Willing to participate and sign informed consent
You will not qualify if you...
- History of other malignant tumors within the last 5 years
- Received neoadjuvant therapy before surgery
- Postoperative incision margin classified as R1 or R2
- Blood transfusion within 2 weeks before surgery
- Having systemic inflammatory response syndrome
- Serious diseases affecting heart, lungs, kidneys, or brain
- Participated in other clinical trials and taken experimental drugs within 30 days
- Incomplete or unsuitable sample collection
- Considered unsuitable for participation by researchers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Shanghai Pulmonary Hospital
Shanghai, Shanghai Municipality, China, 200433
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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