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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03742856
Other study ID # EOC-OMICS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 10, 2018
Est. completion date November 23, 2020

Study information

Verified date November 2018
Source Peking Union Medical College Hospital
Contact Lei Li, M.D.
Phone 13911988831
Email lileigh@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to analyze the multi-omics results between epithelial ovarian cancer (EOC) patient with different FIGO stages and pathological subtypes. The multi-omics profiles include whole exome sequencing, analysis of transcriptomics and metabolomics. A comprehensive multi-omics will reveal the invasiveness and tumorigenesis of EOC.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date November 23, 2020
Est. primary completion date November 23, 2020
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Confirmed primary epithelial ovarian cancer

- Signed an approved informed consents

- Feasible for biopsy

Exclusion Criteria:

- Not meeting all of the inclusion criteria

Study Design


Intervention

Combination Product:
A multi-omics analysis
A multi-omics analysis including whole exome sequencing, transcriptomics and metabolomics.

Locations

Country Name City State
China Lei Li Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Lei Li

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequencies of somatic driving mutations The differences of frequencies of somatic driving mutations will be compared between patients of different FIGO stages and different pathological subtypes. Two years
Secondary Frequencies of alteration of RNA expression The alteration of RNA expression, including mRNA, miRNA, and lncRNA, will be compared between patients of different FIGO stages and different pathological subtypes. Two years
Secondary Frequencies of alteration of protein expression and signal pathway The alteration of patterns of protein expression and signal pathway will be compared between patients of different FIGO stages and different pathological subtypes. Two years
Secondary Progression-free survival Progression-free survival between patients with differential expressed multi-omics will be compared. Five years
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