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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02869269
Other study ID # KUH1160096
Secondary ID
Status Completed
Phase N/A
First received July 15, 2016
Last updated January 26, 2018
Start date October 2015
Est. completion date October 2016

Study information

Verified date January 2018
Source Konkuk University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Previous studies have shown that colorectal cancer patients' prognosis and overall survival was related with immune cell expression in patients' tissue. However, the circulating immune cell activity changes in patients' blood has few studies. The purpose of this study is to analyze the variation of circulating immune cell activity in colorectal patients' blood which is classed as clinical staging.


Description:

The patients were classed as clinical staging

1. Early (stage1+2) and Late(stage3+4)

2. regional lymph node metastasis

3. Distant metastasis

4. TNM stage


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- patient who was planned to undergo colorectal cancer surgery.

Exclusion Criteria:

- age < 20 years old

- history of hypersensitivity reaction in propofol or sevoflurane

- history of previous cancer

- patient with ongoing inflammation

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Early stage
patients who classed as clinical stage 1 and 2
Late stage
patients who classed as clinical stage 3 and 4

Locations

Country Name City State
Korea, Republic of Konkuk University Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Konkuk University Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Other CD4 and Treg cell activity and change of percentage of CD39 and CD73 change of expression level of CD4 and Treg cell activity and change of percentage of CD39 and CD73(0~100 %) preoperative time
Primary Circulating helper T cell activity change of expression level of T cell (0~100 %) preoperative time
Secondary Cytotoxic T cell and natural killer cell activity change of expression level Cytotoxic T cell and natural killer cell(0~100 %)from 0 to 100) preoperative time
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