Quality of Life Clinical Trial
Official title:
Comparison of Postoperative Anal Function Between Different Anastomosis Techniques(Parks Versus Bacon) in Low Rectal Cancer: A Prospective, Multicentric and Randomized Controlled Study
NCT number | NCT05943444 |
Other study ID # | E2023072 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | August 8, 2023 |
Est. completion date | August 8, 2027 |
The goal of this study is to compare the postoperative anal function of patients with ultra-low rectal cancer after Parks operation (colon anal anastomosis) and Bacon operation (colon anal pull-out anastomosis), which may provide clinical evidence for the improvement of anal function and quality of life. The main questions it aims to answer are: the difference of anal function 1 year after surgery type of study: clinical trial participant population: patients with low rectal cancer Participants will receive Parks operation of Bacon operation If there is a comparison group: Researchers will compare Parks and Bacon operation to see if the anal function 1 year after surgery is different.
Status | Recruiting |
Enrollment | 256 |
Est. completion date | August 8, 2027 |
Est. primary completion date | August 8, 2027 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: 1. Men or women, aged between 18 and 75 years; 2. Pathological diagnosis of rectal cancer before operation, with the distance from the lower edge of the tumor to the dentate line = 3cm by MR imaging; 3. No local complications (including complete/ incomplete obstruction, active bleeding, local invasion of sphincter or levator ani, etc.) before operation; 4. Suitable for anal preservation surgery discussed by MDT; 5. Adequate bone marrow, liver, renal and cardiac function meeting the requirements of surgery and anesthesia; 6. R0 resection is expected technically; 7. Provision of written informed consent. Exclusion Criteria: 1. Previous history of malignant colorectal tumors; 2. Complications such as obstruction and gastrointestinal bleeding that need an emergency operation; 3. Unachievable R0 resection due to invasion of adjacent organs by primary tumor; 4. Multiple primary tumors; 5. History of other malignancy; 6. Participation in other clinical trials within the previous 4 weeks of enrollment; 7. ASA physical status score = IV level and/or ECOG performance status = 2; 8. Intolerance of surgery due to liver, renal, cardiopulmonary or coagulation dysfunction, or underlying diseases; 9. History of serious mental disorders; 10. Women in pregnancy or lactation period; 11. Uncontrolled infection before operation; 12. Unsuitable to be included due to other clinical and laboratory conditions by the judgement of investigators. |
Country | Name | City | State |
---|---|---|---|
China | The Sixth Affiliated Hospital, Sun Yatsen University | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Sixth Affiliated Hospital, Sun Yat-sen University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Low Anterior Resection Syndrome (LARS) score 1 year after surgery | use a scoring system for bowel dysfunction after LAR for rectal cancer on the basis of symptoms and impact on quality of life | 1 year after surgery | |
Secondary | LARS score at 3 months after surgery | to score bowel dysfunction after LAR | 3 months after surgery | |
Secondary | LARS score at 6 months after surgery | to score bowel dysfunction after LAR | 6 months after surgery | |
Secondary | Postoperative Quality of Life Score | using a score system to access the quality of life after surgery | 3, 6, and 12 months after operation | |
Secondary | The incidence of postoperative anastomotic complications | the corresponding complications after surgery | 3, 6, and 12 months after operation |
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