Rectal Cancer Clinical Trial
Official title:
An Exploratory Study on the Recovery of Intestinal Flora and Intestinal Function by Preventing Stoma Discharge Reinfusion After Sphincter Preservation for Middle and Low Rectal Cancer
To analyze the occurrence of defecation complications, rectal function, and quality of life indicators after sphincter-preserving surgery for middle and low rectal cancer, the stoma exudate was collected before the stoma was restored, and the defecation complications, rectal function and quality of life indicators were evaluated. The effect of anal reinfusion of stoma discharge on the recovery of intestinal function in patients.
Status | Not yet recruiting |
Enrollment | 30 |
Est. completion date | June 1, 2026 |
Est. primary completion date | June 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: 1. Age: 18~75 years old, male or female; 2. The pathological diagnosis of preoperative biopsy was rectal adenocarcinoma; 3. The clinical stage is T1-4aN0-2M0; 4. No distant multiple metastasis; 5. ECOG score 0-2; 6. Heart, lung, liver and kidney function can tolerate surgery; 7. The clinical diagnosis of middle-low rectal cancer, the lower edge of the tumor is within 10cm from the anal verge, the patients who are to undergo radical rectal resection and prophylactic ileostomy in stage I and intestinal closure in stage II; 8. Patients and their families can understand and be willing to participate in this clinical study, and sign the informed consent. Exclusion Criteria: 1. Past history of malignant colorectal tumor or recent diagnosis with other malignant tumors; 2. Patients with intestinal obstruction, intestinal perforation, intestinal bleeding, etc. requiring emergency surgery; 3. Adjacent organs need combined organ resection; 4. ASA grade = grade IV and/or ECOG performance status score > 2 points; 5. Patients with severe liver and kidney function, cardiopulmonary function, coagulation dysfunction or combined with serious underlying diseases who cannot tolerate surgery; 6. Have a history of serious mental illness; 7. Pregnant or lactating women; 8. Those who have a history of taking hormone drugs; 9. Patients with other clinical and laboratory conditions considered by the researchers should not participate in the trial; 10. There are signs of infection 1 week before the operation, the body temperature is higher than 37.5?, and the blood WBC is higher than 10.0×109/L; 11. There is a history of antibiotic use 1 week before surgery (excluding preoperative shock drugs); 12. Preoperative neoadjuvant patients. |
Country | Name | City | State |
---|---|---|---|
China | Jilin University First Hospital | Changchun | Jilin |
Lead Sponsor | Collaborator |
---|---|
The First Hospital of Jilin University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of low anterior resection syndrome | Incidence of low anterior resection syndrome one month after surgery | one month after surgery | |
Secondary | Incidence of low anterior resection syndrome | Incidence of low anterior resection syndrome 3 months after stoma reversal | 3 months after stoma reversal | |
Secondary | Wexner score | The Wexner score includes 6 dimensions, including sanitary pads, solids, and liquids, with a total score of 20. The score is proportional to the patient's degree of anal incontinence. | 3 months after stoma reversal | |
Secondary | Quality of life score | The EORTCQLQ-C30 scale is a cross-cultural and cross-country QOL-C30 (Quality of Life Questionnare-Core 30) launched by the European Organization for Research on Cancer Treatment (EORTC: The European O-rganization for Reasearch and Treatment of Cancer) in 1993. ), to evaluate QOL from a multi-dimensional perspective, which can better reflect the connotation of QOL, and has been applied to the measurement of QOL of cancer patients in many European countries and regions. | 3 months after stoma reversal |
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