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Completed

NCT Number: NCT06454201

Robotic Natural Orifice Specimen Extraction Surgery Compared to Robotic Assisted Surgery for Median Rectal Cancer

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

the First Affiliated Hospital of Nanchang University

Nanchang, Jiangxi, 330000, China

About this study

A major concern to the safety of the public's health is the prevalence of colorectal cancer, which is the third most prevalent cancer and has a very high fatality rate. There are multiple treatments for rectal cancer, and surgery remains one of the most important ways. Laparoscopic surgery as a minimally invasive technique for the treatment of colorectal has been confirmed by many studies to ensure its safety and reliability. Laparoscopic surgery has also been widely used in clinical. So far, NOSES, as an emerging minimally invasive technology, has caused heated discussions in the minimally invasive surgical community, especially in rectal surgery, the emergence of NOSES, which solves the problems caused by incisions in traditional surgery, improves the mental health of patients, and has good short-term efficacy. In recent years, the popularity of robotic colorectal cancer surgery has been rising, and the concepts of radical treatment, precision, and minimally invasive have been continuously refined, and NOSES surgery, as an emerging minimally invasive technology, has further reduced the impact of surgical trauma on the body, eliminated abdominal scar incision, and avoided complications related to abdominal wall incision, and has been widely used and carried out. In addition to the benefits of patients, the high-definition lens of the robotic surgery system and the flexible robotic arm greatly remove the trembling of the operator's hand, improve the flexibility and accuracy of the operator's operation, and are more conducive to challenging operations in narrow spaces. Compared with laparoscopy, the robotic surgical system has great advantages in some aspects, such as postoperative patient urination function, sexual function, surgical complications. Robotic surgical systems, combined with NOSES, may bring greater benefits to patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

robotic natural orifice specimen extraction surgery

Procedure

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 transabdominal specimen extraction surgery

Procedure

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.

Primary outcomes

  1. The rate of all complications

    Time frame: 1 months after surgery

    incidence rate

  2. The rate of all complications (Clavien-Dindo grade ≥ III )

    Time frame: 1 months after surgery

    incidence rate

  3. The rate of anastomotic complications

    Time frame: 1 months after surgery

    Anastomotic leakage and anastomotic bleeding

Secondary outcomes

  1. operative time

    Time frame: Intraoperative

    minutes

  2. estimation of blood loss

    Time frame: Intraoperative

    milliliters

  3. postoperative hospital stay

    Time frame: 1 day after operation

    days

  4. visual analogue pain score

    Time frame: 1 weeks after surgery

    score

Sponsors and collaborators

Lead sponsor

Nanchang University

Other

Registry information

Official study title

the First Affiliated Hospital of Nanchang University

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Jun 12, 2024
Registry last updated
Jan 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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