None listed
Conditions
Interventions
None listed
Sponsors
Inje University Busan Paik Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - experimental group(C): Patients undergoing colorectal cancer surgery or intestinal reconstruction under general anesthesia, Patients with a history of chemotherapy within 12 months before surgery, aged 18 to 75 years, BMI 18-29 kg/m2, and American Society of. Anesthesiologists(ASA) physical status1, 2. - control group(N): Patients undergoing colorectal cancer surgery or intestinal reconstruction under general anesthesia, Patients without a history of chemotherapy before surgery, aged 18 to 75 years, BMI 18-29 kg/m2, and American Society of. Anesthesiologists(ASA) physical status1, 2.
Exclusion criteria
Exclusion criteria: Patients with neurological, neuropsychiatric history, taking sadatives, taking chronic alcohol, who is expected to be difficult to maintain airway, difficult to communicate, or with a history of chomotherapy before the surgery 13 months prior to surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Median effective effect-site concentration of propofol causing loss of consciousness | — |
Secondary
| Measure | Time frame |
|---|---|
| Modified observer’s assessment of alertness/sedation scale | — |
Countries
Korea, Republic of
Contacts
Public ContactSeunghee Ki
Inje University Busan Paik Hospital
Outcome results
None listed