Thoracic Surgery by SHURUI Single-Port Surgical Robot

NCT07255703 | Not Yet Recruiting

• 1 other identifier: KF-600-3-583
• Study Type: observational
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

The introduction of single-port surgical robot has been a transformative breakthrough in the medical field, representing a significant advancement in minimally invasive procedures. One notable innovation is the SHURUI single-port surgical robot (SP), developed by Beijing Surgerii Robotics Company Limited. The SHURUI SP represents a cutting-edge technology in the field. This system features snake-like surgical instruments utilizing "dual continuum mechanism", which enables precise single-port procedures with wide range of motion and high load capacity. The SHURUI SP has been cleared by the National Medical Products Administration (NMPA) of China for use in urology and gynecology and has completed clinical trials for general surgery and thoracic surgery. It is China's first and the world's second approved single-port surgical robot. Compared to multi-port surgical robots, it can provide patients with less trauma, fewer complications, and faster recovery. The SHURUI SP has also achieved significant breakthroughs in clinical applications. It conducted the world's first randomized controlled clinical trial on single-port robotic urologic surgery and introduced a series of innovative surgical paradigms. These include the world's first single-port sleeve lobectomy, single-port retroperitoneal adrenalectomy, single-port retroperitoneal partial nephrectomy, single-port distal gastrectomy (Billroth I anastomosis), and single-port total gastrectomy. Our centre is the first robotic surgical centre in Hong Kong since 2005. Over the years, investigators have established our centre to be one of the leading centre in Hong Kong and the region, with involvement in various new development in thoracic robotic procedures, publications and books, and more recently in robotic endo-lumenal procedures. In this study, investigators evaluate the early surgical outcome and objective functional outcome of patients undergoing robotic thoracic surgery by SHURUI SP.

Conditions

Thoracic Surgery

Outcome Measures

Primary Outcomes (2)

• conversion rate

  The feasibility of the Endoscopic Surgical System, SR-ENS-600 for thoracic robotic procedures (Lobectomy, Segmentectomy Wedge resection of lung and Mediastinal Tumour Resection), as measured by the conversion rate

  1 year + 1 month follow-up

• major peri-operative complication rate (Clavein-Dindo grading III or above)

  The safety profile of the Endoscopic Surgical System, SR-ENS-600 for thoracic robotic procedures (Lobectomy, Segmentectomy Wedge resection of lung and Mediastinal Tumour Resection), as measured by the peri-operative complication profile.

  1 year + 1 month follow-up

Secondary Outcomes (11)

• Operation time

  1 year

• Estimated intraoperative blood loss (EBL)

  1 year

• Length of hospital stay

  1 year + 1 month follow-up

• Postoperative pain score

  1 year + 1 month follow-up

• Blood transfusion rate

  1 year

Study Arms (2)

Lobectomy, Segmentectomy Wedge resection of lung

Device: Device: Endoscopic Surgical System, SR-ENS-600

Mediastinal Tumour Resection

Device: Device: Endoscopic Surgical System, SR-ENS-600

Interventions

Device: Endoscopic Surgical System, SR-ENS-600 DEVICE

undergoing robotic thoracic surgery by the Endoscopic Surgical System, SR-ENS-600

Lobectomy, Segmentectomy Wedge resection of lung; Mediastinal Tumour Resection

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients undergoing Lobectomy, Segmentectomy, Wedge Resection of the lung, or Mediastinal Tumour Resection.

You may qualify if:

• Age between 18 - 75 years;
• Subjects need to undergo endoscopic surgery and meet one of the following indications for surgical treatment:
• Lobectomy, segmentectomy wedge resection of lung: Clinically diagnosed resectable early stage non-small cell lung carcinoma; oligometastatic cancer to the lung;
• Mediastinal mass resection: Clinically diagnosed mediastinal tumour (benign or malignant) that are indicated for resection;
• Preoperative ASA grade: Grade I-III;
• Subject voluntarily participates in the clinical trial, and agrees or his/her guardian agrees and signs the informed consent.

You may not qualify if:

• Subjects with a previous history of thoracic surgery or other malignant tumor which, in the judgement of the investigator, make them unsuitable for enrolment;
• Subjects with severe co-morbidities or organ dysfunction (heart, lung, liver, brain, kidney, etc.) or deemed too weak/ unsuitable for general anesthesia or operation;
• Non-correctable coagulopathy and severe bleeding tendency；
• Emergency surgery;
• Severe obesity with BMI ≥30 kg/m2;
• Subjects with severe allergic constitution, suspected or confirmed alcohol, drug addiction;
• Other circumstances in which the investigator considered participation in this clinical trial inappropriate.

Sponsors & Collaborators

• Chinese University of Hong Kong: lead

Study Sites (1)

Prince of Wales Hospital

Shatin, Hong Kong

Location

Central Study Contacts

Calvin Sze Hang Ng

CONTACT

+852 3505 2618; calvinng@surgery.cuhk.edu.hk

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: November 20, 2025
• First Posted: December 1, 2025
• Study Start: April 1, 2026
• Primary Completion (Estimated): November 1, 2026
• Study Completion (Estimated): November 30, 2026
• Last Updated: March 20, 2026

Record last verified: 2026-03

Locations

HK (1)