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Clinical Trials/NCT02567929
NCT02567929
Completed
Not Applicable

Assessment of the Anesthetic Effect on the Activity of Immune Cell in Patient With Breast Cancer

Konkuk University Medical Center1 site in 1 country218 target enrollmentMarch 2016

Overview

Phase
Not Applicable
Intervention
propofol group
Conditions
Breast Cancer
Sponsor
Konkuk University Medical Center
Enrollment
218
Locations
1
Primary Endpoint
CD39 and CD73 on circulating regualtory T cells
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Anesthetics agents has variety inflammation during the cancer surgery. This perioperative inflammation can influence to cancer metastasis or recurrence.

The purpose of this study is to prove the variation of immune cell activity between preoperative and postoperative period.

Detailed Description

The patients were allocated randomly to receive propofol or sevoflurane. Also, a total of 18ml of blood sample was obtained for total 3 times in consecutive order. 1. immediate before anesthesia induction 2. postoperative 1 hours 3. postoperative 24 hours Serum in blood will be obtained and activity of helper T cell, natural killer cell and level of serum cytokine will be evaluated by flow cytometry or enzyme-linked immunosorbent assay

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
December 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Factorial
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Seong-Hyop Kim

Associate Professor

Konkuk University Medical Center

Eligibility Criteria

Inclusion Criteria

  • patient who was planned to undergo colon cancer surgery.

Exclusion Criteria

  • age \< 20 years old
  • history of hypersensitivity reaction in propofol or sevoflurane
  • history of previous cancer
  • patient with ongoing inflammation

Arms & Interventions

propofol group

The patient who anesthetized by using propofol.

Intervention: propofol group

sevoflurane group

The patient who anesthetized by using propofol

Intervention: sevoflurane group

Outcomes

Primary Outcomes

CD39 and CD73 on circulating regualtory T cells

Time Frame: preoperative time. postoperative 1 hours and 24 hours

change of percentage of CD39 and CD73 (scores range from 0 to 100)

Secondary Outcomes

  • Circulating natural killer cells(preoperative time. postoperative 1 hours and 24 hours)

Study Sites (1)

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