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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02567929
Enrollment
218
Registered
2015-10-05
Start date
2016-03-31
Completion date
2016-12-31
Last updated
2018-04-02

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

Conditions

Breast Cancer

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

Interventions

DRUGpropofol group

Patient will be anesthetized by using propofol infusion during operation.

Patient will be anesthetized by using sevoflurane inhalation during operation.

Sponsors

Konkuk University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
CD39 and CD73 on circulating regualtory T cellspreoperative time. postoperative 1 hours and 24 hourschange of percentage of CD39 and CD73 (scores range from 0 to 100)

Secondary

MeasureTime frameDescription
Circulating natural killer cellspreoperative time. postoperative 1 hours and 24 hourschange of percentage of circulating natural killer cell (scores range from 0 to 100)

Other

MeasureTime frameDescription
Circulating type 1 and type 17 helper T cellspreoperative time. postoperative 1 hours and 24 hourschange of percentage of helper T cell (scores range from 0 to 100)

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026