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Detection kit of the combination of methylated SDC2 and TFPI2 (fluorescence PCR method)

Study the clinical practice of SDC2 and TFPI2 methylation in the early detection of colorectal cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100050110
Enrollment
Unknown
Registered
2021-08-16
Start date
2020-12-30
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

Colorectal Cancer

Interventions

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Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
21 Years to 80 Years

Inclusion criteria

Inclusion criteria: Colorectal cancer enrollment requirements: 1. Adult population aged 18 years or older; 2. Patients who are clinically diagnosed as requiring colonoscopy and who are scheduled to undergo colonoscopy soon; 3. patients with high suspicion of colorectal cancer diagnosed by colonoscopy or pathological biopsy, and who have not undergone surgery and histopathological examination. For patients with interfering disease other than bowel cancer, the entry requirements are 1. aged 18 years or older in the adult population; 2. patients with other gastrointestinal cancers (including esophageal cancer, gastric cancer, liver cancer, pancreatic cancer, bile duct cancer, etc.) and other benign gastrointestinal diseases (including esophagitis, gastritis, enteritis, inflammatory bowel disease, appendicitis, peptic ulcer, colorectal polyps, colorectal adenoma, hemorrhoids, etc.) who are scheduled to undergo colonoscopy or already have colonoscopy results and are untreated.

Exclusion criteria

Exclusion criteria: Exclusion Criteria Any of the following conditions can be excluded if any of the following are met. (1) Unclear pathological results. (2) The sample has been contaminated, not preserved as required, or the sample volume is insufficient. (3) Incomplete medical history information. (4) Samples with insufficient total extracted DNA samples (5) Samples whose internal control Ct still does not meet the quality control requirements after sample retesting.

Design outcomes

Primary

MeasureTime frame
Sensitivity;Specificity;Accuracy;Kappa;

Countries

China

Contacts

Public ContactYaling Dou

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

pumchdyl67@163.com+86 13651332582

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026