NCT06454201

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

June 6, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 12, 2024

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

January 30, 2026

Status Verified

June 1, 2025

Enrollment Period

3 years

First QC Date

June 6, 2024

Last Update Submit

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 COMPARATOR

After 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.

Procedure: robotic natural orifice specimen extraction surgery

robotic transabdominal specimen extraction surgery for middle rectal cancer

SHAM COMPARATOR

After internal mobilization, the tumor segment of the bowel was removed through an abdominal incision. Excise the tumor segment of the bowel outside the incision.

Procedure: robotic transabdominal specimen extraction surgery

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.

robotic natural orifice specimen extraction surgery for middle rectal cancer

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.

robotic transabdominal specimen extraction surgery for middle rectal cancer

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Study Officials

  • shanping Ye

    The First Affiliated Hospital of Nanchang University

    STUDY CHAIR

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

Locations