Anastomotic Stenosis Clinical Trial
Official title:
A Prospective Clinical Study of Transanal and Transabdominal Combined Endoscopic Resection of Rectal Stenosis and Anal Reconstruction for Severe Rectal Anastomotic Stenosis
Severe rectal anastomotic stenosis can not only cause intestinal obstruction, but also be accompanied by frequent defecation, which affects the quality of life, and patients face the outcome of permanent stoma or temporary stoma again. Traditional transabdominal resection and reconstruction of rectal anastomotic stenosis is more likely to occur due to unclear anatomical structure, dense scars around the intestinal canal, complications such as ureteral and urethral injury and massive presacral hemorrhage. In addition,41%of patients with anastomotic stenosis who underwent reoperation through abdominal surgery had anastomotic leakage again, and up to 30% of patients could not close the stoma. The advantages of transanal total mesorectal excision (taTME) using a transanal approach for total mesorectal excision in the treatment of middle and low rectal cancer with difficult pelvis have been demonstrated by our group. However, taTME has rarely been explored in the treatment of anastomotic stenosis. Our team retrospectively summarized the patients who underwent transabdominal transanal endoscopic resection and reconstruction of anastomotic stenosis (l-taTME), and initially demonstrated the safety and effectiveness of this surgical method, with a stoma closure rate of 90%. Although the advantages of l-taTME in the treatment of severe rectal anastomotic stenosis are obvious in theory and preliminary clinical practice, there is a lack of prospective studies. Therefore, the investigators plan to conduct a prospective clinical study to observe the safety and efficacy of l-taTME reconstruction surgery, and to provide high-level evidence-based medical basis for the selection of resection and reconstruction surgery for patients with rectal anastomotic stenosis.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | December 31, 2026 |
Est. primary completion date | December 31, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: 1. Age of 18-70 years old; 2. ECOG performance status score 0-2; 3. previous rectal resection; 4. patients diagnosed with middle and low rectal anastomotic tubular stenosis; 5. can tolerate general anesthesia; 6. The subjects and their family members, who could understand the study protocol and were willing to participate, signed the informed consent form. Exclusion Criteria: 1. patients with acute intestinal obstruction, intestinal perforation or intestinal bleeding requiring emergency surgery; 2. severe pelvic adhesion and frozen pelvis; 3. patients with unstable primary tumors or combined with tumors at other sites; 4. previous history of left hemicolectomy; 5. ASA grade IV to V; 6. combined organ resection; 7. severe mental illness; 8. pregnant or lactating women; 9. severe cardiovascular disease, uncontrolled infection or other uncontrolled comorbidities; |
Country | Name | City | State |
---|---|---|---|
China | Sixth Affiliated Hospital of Sun yat-sen University | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Sun Yat-sen University |
China,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Stoma recovery rate | whether the stoma recovery and restoration of bowel continuation | 3 months after surgery | |
Secondary | incidence of postoperative anastomotic leakage | whether the occurence of anastomotic leakage | 1 month after surgery | |
Secondary | incidence of postoperative anastomotic bleeding | whether the occurence of anastomotic bleeding | Duration of 7 days after surgery | |
Secondary | Incidence of severe bowel dysfunction | Low Anterior Resection Syndrome Score (0-20: No LARS 21-29: Minor LARS 30-42: Major LARS) | 3 months after stoma recovery | |
Secondary | Incidence of severe bowel dysfunction | Low Anterior Resection Syndrome Score (0-20: No LARS 21-29: Minor LARS 30-42: Major LARS) | 6 months after stoma recovery | |
Secondary | Incidence of severe bowel dysfunction | Low Anterior Resection Syndrome Score (0-20: No LARS 21-29: Minor LARS 30-42: Major LARS) | 1 year after stoma recovery | |
Secondary | Incidence of severe bowel dysfunction | Low Anterior Resection Syndrome Score (0-20: No LARS 21-29: Minor LARS 30-42: Major LARS) | 2 years after stoma recovery | |
Secondary | Anorectal function | Anorectal pressure Rectal sensory function Rectoanal reflex function | 1 year after stoma recovery | |
Secondary | Anorectal function | Anorectal pressure Rectal sensory function Rectoanal reflex function | 2 year after stoma recovery | |
Secondary | bowel function | Memorial Sloan-Kettering Cancer Center bowel function instrument | 3 months after stoma recovery | |
Secondary | bowel function | Memorial Sloan-Kettering Cancer Center bowel function instrument | 6 months after stoma recovery | |
Secondary | bowel function | Memorial Sloan-Kettering Cancer Center bowel function instrument | 1 year after stoma recovery | |
Secondary | bowel function | Memorial Sloan-Kettering Cancer Center bowel function instrument | 2 year after stoma recovery | |
Secondary | Quality of life evaluation after stoma closure | European Organization for Research and Treatment of Cancer QLQ-C30 (0-100 0:poor 100:best) | 3 months | |
Secondary | Quality of life evaluation after stoma closure | European Organization for Research and Treatment of Cancer QLQ-C30 (0-100 0:poor 100:best) | 6 months | |
Secondary | Quality of life evaluation after stoma closure | European Organization for Research and Treatment of Cancer QLQ-C30 (0-100 0:poor 100:best) | 1 year | |
Secondary | Quality of life evaluation after stoma closure | European Organization for Research and Treatment of Cancer QLQ-C30 (0-100 0:poor 100:best) | 2 years | |
Secondary | Quality of life evaluation after stoma closure | European Organization for Research and Treatment of Cancer QLQ-C30 (0-100 0:poor 100:best) | 3 years | |
Secondary | Inraoperative condition | operation time and whether to convert to laparotomy | In the process of operation | |
Secondary | Perioperative recovery time | Duration of analgesics in hours For the first time the exhaust time in hours Time to first defecation in hours Time to first fluid intake in hours Time to resume normal diet in hours Abdominal drainage tube removal time in days Catheter removal time in days Length of postoperative hospital stay in days | perioperative period |
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