Actively Recruiting
ctDNA Methylation Application in Postoperative Relapse and Adjuvant Chemotherapy Efficacy Evaluation
Led by Singlera Genomics Inc. · Updated on 2024-05-22
2000
Participants Needed
1
Research Sites
325 weeks
Total Duration
On this page
Sponsors
S
Singlera Genomics Inc.
Lead Sponsor
S
Second Affiliated Hospital, School of Medicine, Zhejiang University
Collaborating Sponsor
AI-Summary
What this Trial Is About
In this study, the investigators aimed to apply their previously developed multi-locus blood-based assay targeting circulating tumor DNA methylation to monitor postoperative relapse and evaluate adjuvant chemotherapy efficacy in resected stage I and stage II (without high risk) colorectal cancer after radical resection.
CONDITIONS
Official Title
ctDNA Methylation Application in Postoperative Relapse and Adjuvant Chemotherapy Efficacy Evaluation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histologically confirmed stage I or stage II (without high risk) colorectal cancer
- Male or female aged 18 years or older on the day of signing informed consent
- Positive ctDNA test before colorectal cancer surgery
- Eastern Cooperative Oncology Group (ECOG) performance status of 1 or less
- Ability to provide written informed consent and comply with study requirements
You will not qualify if you...
- Personal history of colorectal cancer, colorectal adenoma, or aerodigestive tract cancer
- Received neoadjuvant systemic therapy before colorectal cancer surgery
- Pregnant or lactating
- Any condition or abnormality that could affect study results or participation, as judged by the Investigator
- Inadequate tumor material quality or quantity to support ctDNA analysis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Second Affiliated Hospital
Hangzhou, Zhejiang, China, 310009
Actively Recruiting
Research Team
H
HongFeng cao, Ph.D
CONTACT
R
Rui Liu, Ph.D
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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