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Microplastics in Paraneoplastic and Intratumoral for Colorectal Cancer

Identification of Paraneoplastic and Intratumoral Microplastics in Colorectal Cancer and Their Association Analysis With Macrogenomics and Metabolomics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07063550
Enrollment
100
Registered
2025-07-14
Start date
2024-12-01
Completion date
2026-12-31
Last updated
2025-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer (MSI-H), Microplastic Exposure

Keywords

colorectal cancer, microplastic, Paraneoplastic, Genomics, Metabolomics

Brief summary

The objective of this study is to identify and characterize microplastics present in peritumoral and intratumoral tissues of colorectal cancer patients, and to investigate their associations with gut microbiome composition and metabolic profiles. By integrating microplastic analysis with metagenomic and metabolomic data, we aim to explore the potential impact of environmental microplastic exposure on tumor microenvironment alterations, microbial dysbiosis, and metabolic reprogramming in colorectal cancer.

Interventions

OTHERexposure to microplastic

Microplastic content in cancerous and paracancerous tissues

Sponsors

Dong Peng
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients (≥18 years old) with histologically confirmed colorectal adenocarcinoma. * Undergoing elective radical colorectal cancer resection at the study hospital. * No prior chemotherapy, radiotherapy, or targeted therapy before surgery. * Availability of both tumor tissue and adjacent normal (peritumoral) tissue samples during surgery. * Willingness to provide stool and/or blood samples for metagenomic and metabolomic analysis. * Ability to understand the study procedures and provide written informed consent.

Exclusion criteria

* Patients with a history of other malignancies within the past 5 years. * Emergency surgery due to obstruction, perforation, or bleeding. * Inadequate sample quality or volume for microplastic, metagenomic, or metabolomic analysis. * Presence of chronic inflammatory bowel disease (e.g., Crohn's disease or ulcerative colitis). * Use of antibiotics, probiotics, or prebiotics within 4 weeks prior to sample collection. * Pregnant or breastfeeding women. * Refusal or inability to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
genomicsBlood specimens were obtained within one week prior to surgery.Genomics was tested by preoperative blood specimens.

Secondary

MeasureTime frameDescription
metabolomicsBlood specimens were obtained within one week prior to surgery.Metabolomics was tested by preoperative blood specimens.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026