Colorectal cancer
Conditions
Interventions
The participation start date is the time of consent to this research, observation start time is the start of observation, and observation end time is the time of the end of surgery. In the case of Pr
Sponsors
Hiroshima University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients whose age at agreement acquisition is from 20 years old to 80 years old. 2. Patients who are scheduled to undergo laparoscopic assisted colorectal resection at our hospital due to hospitalization (degree of progression of colorectal cancer does not matter). 3. Patient whose PS (ECOG) are either 0 or 1. 4. Patients whose main organ function are maintained. Fulfill all of the following laboratory findings. (Use the latest inspection value within 30 days of registration) 1.T.bil less than 1.5 mg/dL 2.AST(GOT) less than 200 IU/L 3.ALT(GPT) less than 200 IU/L 4.Cr less than 1.2 mg/dL 5. Patients who obtain written consent regarding the participation of this study.
Exclusion criteria
Exclusion criteria: 1. Patients with a history of abdominal surgery 2. Patients who are undergoing or plan to conduct anticoagulation therapy before and during surgery 3. Patients with a history of ischemic heart disease, cerebral infarction. 4. Patients judged by the research doctor to be inappropriate for participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| All adverse events during perioperative time. | — |
Countries
Japan
Contacts
Public ContactShoichiro Mukai
Graduate school of Hiroshima University Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomed
Outcome results
None listed