Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:24 AM
Ignite Modification Date:
2025-12-25 @ 1:24 AM
NCT ID:
NCT05125393
Eligibility Criteria:
Inclusion Criteria:
* Patients with locally advanced colorectal cancer met the following criteria at the time of enrollment:
1. Adult male and female, aged between 18-75 years
2. Colonoscopic biopsy confirmed colonic adenocarcinoma
3. Before treatment, the tumor was located between ileocecal part and ascending colon liver area
4. There were no local complications (no complete obstruction, no massive active bleeding, no perforation and abscess formation) before operation
5. The functions of heart, lung, liver and kidney meet the requirements of operation and anesthesia
6. Informed consent form be signed
Exclusion Criteria:
* Patients who met the following criteria at the time of inclusion were excluded from this trial:
1. Previous history of malignant colorectal tumor
2. Patients with intestinal obstruction, intestinal perforation and intestinal bleeding requiring emergency surgery
3. The primary tumor invades the abdominal wall and / or adjacent organs, resulting in inability to R0 resection
4. Unresectable lymph node metastasis
5. Recent diagnosis complicated with other malignant tumors
6. Patients who had participated or were participating in other clinical trials within 4 weeks before enrollment
7. American Society of Anesthesiologists (ASA) physical status classes ≥ grade IV and / or Eastern Cooperative Oncology Group (ECOG) physical state score ≥ 2 points (see Appendix for details)
8. Patients with severe liver and kidney function, cardiopulmonary function, coagulation dysfunction or combined with serious basic diseases can not tolerate the operation
9. Have a history of serious mental illness
10. Pregnant or lactating women
11. Patients with uncontrolled infection before operation
12. Some researchers believe that patients with other clinical and laboratory conditions should not participate in the trial
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT05125393
Study Brief:
Protocol Section:
NCT05125393