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Anesthesia, TIVA, Balanced Anesthesia, NK Cell

The Differences Between the Effects of Total Intravenous Anesthesia (TIVA) and Balanced Anesthesia on NK Cell and Cytokine Response in Colorectal Cancer Patients Undergoing Cytoreductive Surgery and HIPEC(Hyperthermic Intraperitoneal Chemotherapy)

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05951842
Enrollment
0
Registered
2023-07-19
Start date
2018-04-16
Completion date
2020-02-28
Last updated
2023-07-19

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

Conditions

Colorectal Cancer

Brief summary

Anesthetic method was reported to have an impact on postoperative long-term outcome in cancer patients. In this study, we will investigate the effect of different anesthetic methods on NK cell activity, cytokine response and postoperative outcome in colorectal cancer patients undergoing CRS and HIPEC. We will compare propofol-based total intravenous anesthesia (TIVA) with balanced anesthesia to determine the effect of propofol, inhalation agent, and opioid on tumor genesis, recurrence, NK cell activity, cytokine response, and postoperative outcome.

Interventions

DRUGanesthetic method

Patients will be assigned to one of the groups, TIVA group or Balanced anesthesia group. In TIVA group, anesthesia will be maintained by propofol and remifentanil infusion under target controlled infusion. In contrast, anesthesia will be maintained by sevoflurane and remifentanil infusion in the balanced anesthesia group.

Sponsors

Gangnam Severance Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Colorectal cancer patients undergoing elective cytoreductive surgery and HIPEC (20-70 yrs old) 2. American Society of Anesthesiologists physical status I, II, III

Exclusion criteria

1. Patients under 20 years old. 2. Patients with long-term steroid therapy or immunosuppressive therapy. 3. Patients with long-term NSAIDs therapy. 4. Patients who cannot communicate with other person or with cognitive disorder. 5. Patients who cannot read the consent form.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative immune function (NK cell count)Postoperative day 1Postoperative immune function will be measured at baseline, POD#1, and POD#7. Postoperative immune function will be investigated by measuring NK cell count.

Outcome results

None listed

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