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Study on the methylation of three genes, MT-1A, Epo and Septin9, in the auxiliary diagnosis of esophageal cancer

MT-1A,Epo and Septin9 Genes Methylation Detection Kit for Human Esophageal Cancer (Real-Time PCR)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083525
Enrollment
Unknown
Registered
2024-04-26
Start date
2022-03-11
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

esophageal cancer

Interventions

Gold Standard:Gastrointestinal endoscopy and/or pathological diagnosis
Index test:Qualitative detection of MT-1A gene ,Epo gene and Septin9 gene methylation in human plasma.

Sponsors

Cancer Hospital Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1) The sample information is complete, including sample medical record number, gender, age, clinical diagnosis information, etc.; 2) The plasma volume is not less than 2.0mL, and the blood sample is visually observed, and there is no visible turbidity or insoluble matter; 3) The subject signs an informed consent Book. 4) Anyone who meets one of the following conditions can be enrolled, as follows: ? People who are preparing for esophageal cancer surgery or esophagoscopy and have no history of esophageal cancer surgery or radiotherapy and chemotherapy; ? People who have been diagnosed with or without other esophageal diseases Population; ? People who have been diagnosed with other cancers; ? Some subjects whose plasma volume meets 4.0mL are enrolled (assessment reagent testing and first-generation sequencing are performed at the same time); ? Some subjects who are the same before and after surgery are enrolled.

Exclusion criteria

Exclusion criteria: 1) Samples that were not collected and stored in accordance with the [Sample Collection Requirements]; 2) The sample size is insufficient to complete the test; 3) The sample information is incomplete (including sample medical record number, gender, age, clinical diagnosis information, etc.); 4) Researchers think any other situation where it is considered inappropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
sensitivity;Specificity;Kappa value;

Countries

China

Contacts

Public ContactLi Yin

Cancer Hospital Chinese Academy of Medical Sciences

zhu.zhenyu@biochainbj.com+86 10 6790 2809

Outcome results

None listed

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