Robotic Natural Orifice Specimen Extraction Surgery Compared to Robotic Assisted Surgery for Median Rectal Cancer
the First Affiliated Hospital of Nanchang University
1 other identifier
interventional
150
1 country
1
Brief Summary
The purpose of this study is to evaluate the short-term outcomes of roboric natural orifice specimen extraction surgery (NOSES-II) compared to conventional assisted robotic surgery in the treatment of median rectal cancer. The main question it aims to answer is: is it safe and feasible to perform roboric natural orifice specimen extraction surgery (NOSES-II) for median rectal cancer? What are the advantages of roboric natural orifice specimen extraction surgery (NOSES-II) compared to conventional assisted robotic surgery for median rectal cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2023
CompletedFirst Submitted
Initial submission to the registry
June 6, 2024
CompletedFirst Posted
Study publicly available on registry
June 12, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedJanuary 30, 2026
June 1, 2025
3 years
June 6, 2024
January 28, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
The rate of all complications
incidence rate
1 months after surgery
The rate of all complications (Clavien-Dindo grade ≥ III )
incidence rate
1 months after surgery
The rate of anastomotic complications
Anastomotic leakage and anastomotic bleeding
1 months after surgery
Secondary Outcomes (4)
operative time
Intraoperative
estimation of blood loss
Intraoperative
postoperative hospital stay
1 day after operation
visual analogue pain score
1 weeks after surgery
Study Arms (2)
robotic natural orifice specimen extraction surgery for middle rectal cancer
ACTIVE COMPARATORAfter the body is free, the tumor segment of the bowel is pulled out through the anus. Excise the tumor segment of the colon outside the anus.
robotic transabdominal specimen extraction surgery for middle rectal cancer
SHAM COMPARATORAfter internal mobilization, the tumor segment of the bowel was removed through an abdominal incision. Excise the tumor segment of the bowel outside the incision.
Interventions
After the rectum and its mesorectum were dissociated, the rectum was transected at 2 cm below the tumor by using a linear stapler. Then the rectal stump was incised and disinfected with iodophor, the protective sleeve was placed into the abdominal cavity through the assistant hole. An assistant delivered oval forceps into the pelvic cavity through the anus and used oval forceps to grip one end of the protective sleeve. Then slowly pulled out the protective sleeve. Eventually, one end of the protective sleeve was placed inside the abdominal cavity and the other outside the anus, completely covering the rectal stump and the perianal area. Tumor was pulled out of the rectal stump, then the colon was then disconnected at 10 cm above the tumor. The anvil was placed into the stump of the sigmoid colon and disinfected with iodophor, and then the anvil was delivered into the abdominal cavity. Place a circular stapler through the anus for end-to-end anastomosis of the rectum and sigmoid colon.
After the rectum and its mesorectum were dissociated, the rectum was transected at 2 cm below the tumor by using a linear stapler. Take a 6cm incision through the rectus abdominis muscle in the lower left abdomen and place an incision protective cover. Cut off the intestinal tube 10cm from the upper edge of the tumor and place a stapler base. The rectal stump was sutured with purse-string suture. Place a circular stapler through the anus for end-to-end anastomosis of the rectum and sigmoid colon. After completion of digestive tract reconstruction. The pelvic and abdominal cavities were washed repeatedly with normal saline until there were no blood remained. Close the abdominal cavity layer by layer.
Eligibility Criteria
You may qualify if:
- The age is more than 18 years old and less than or equal to 85 years old
- Eastern Cooperative Oncology Group score ≤2
- Preoperative pathological diagnosis of rectal adenocarcinoma
- cT1-3NxM0 median rectal cancer defined by preoperative contrast-enhanced MRI
- The maximum diameter of tumor ≤5cm on preoperative enhanced MRI
- The body can tolerate the operation and sign the informed consent
You may not qualify if:
- multiple primary colorectal cancer
- recurrent rectal cancer
- preoperative neoadjuvant chemoradiotherapy
- complicated with intestinal obstruction or intestinal bleeding requiring emergency surgery
- previous anal surgery history
- BMI≥30kg/m2
- severe mental illness
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
the First Affiliated Hospital of Nanchang University
Nanchang, Jiangxi, 330000, China
Study Officials
- STUDY CHAIR
shanping Ye
The First Affiliated Hospital of Nanchang University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- professor
Study Record Dates
First Submitted
June 6, 2024
First Posted
June 12, 2024
Study Start
January 1, 2023
Primary Completion
December 31, 2025
Study Completion
December 31, 2025
Last Updated
January 30, 2026
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share