Skip to content

A prospective, multicenter, single-arm study evaluating the safety and efficacy of telesurgery Using SHURUI Single-Port Robotic System

A prospective, multicenter, single-arm study evaluating the safety and efficacy of telesurgery Using SHURUI Single-Port Robotic System

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119456
Enrollment
Unknown
Registered
2026-02-27
Start date
2026-03-02
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disease of Digestive System/Urogenital System/Respiratory System

Interventions

Experimental group:SHURUI Single-Port Robotic System

Sponsors

Ruijin Hospital affiliated to Shanghai Jiaotong University School of Medicine (North Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years old, and gender is not limited; 2. Those who are scheduled to undergo any of the following surgeries assisted by the SHURUI Single-Port Robotic System: (1) Gynecological surgeries such as hysterectomy with pelvic lymph node dissection, etc. (2) Urological surgeries such as partial nephrectomy, radical prostatectomy, etc. (3) General surgical procedures such as radical gastrectomy for distal gastric cancer, radical resection of colorectal cancer, hepatectomy/splenectomy, etc. (4) Thoracic surgeries such as segmentectomy/lobectomy, radical resection of esophageal cancer, etc. (5) Others who, as judged by the researcher, have indications for thoracoabdominal endoscopic surgery. 3. Patients fully understand the benefits and risks of this trial, and are willing to participate in this trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Have severe heart, lung, brain, liver and kidney diseases, unable to tolerate surgery or anesthesia; 2. Inability to tolerate pneumoperitoneum; 3. Severe anemia, coagulation dysfunction; 4. Pregnant and lactating women; 5. Those with a history of epilepsy or psychiatric illness; 6. Extensive metastasis in the abdomen-pelvic cavity of the tumor; 7. Severe obesity with BMI >= 30 kg/m^2 8. Participated in clinical trials of other drugs or devices within 3 months before surgery; 9. Other conditions deemed unsuitable by the investigator to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Telesurgery non-conversion rate;Clavien-Dindo Grade III or Higher Complication Rate;

Secondary

MeasureTime frame
Network Transmission Evaluation;Telesurgery Operation Time;Estimate Blood loss;Blood transfusion rate;Surgeon's satisfaction socre;Fluorescence Imaging Quality Evaluation;Postoperation pain score;The length of hospital stay;Evaluation of postoperative incision;Overall 30-Day Postoperative Complication Rate;30-Day Readmission Rate;30-Day Reoperation Rate;30-Day Mortality Rate;Instrument defects incidence;

Countries

China

Contacts

Public ContactRen Zhao

Ruijin Hospital affiliated to Shanghai Jiaotong University School of Medicine (North Hospital)

1217909635@qq.com+86 21 6437 0045

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026