Clinical Trial to Evaluate the Efficacy and Safety of a Thoracic and Abdominal Endoscopic Surgical System

Cornerstone Robotics

Status

Invitation-only

Conditions

Pathologic Stage I Gastric Cancer AJCC v8

Radical Hysterectomy

Esophageal Cancer

Hepatectomy

Colorectal Cancer

Treatments

Procedure: Robot-assisted surgery

Study type

Interventional

Funder types

Industry

Identifiers

NCT06587152

F-00359-002

Details and patient eligibility

About

Evaluation of the efficacy and safety of thoracic and abdominal endoscopic surgical systems manufactured by Shenzhen Cornerstone Robotics Technology Co., Ltd. for use in general, gynaecological and thoracic surgical procedures.

Full description

The trial was designed using a prospective, multi-centre, single-group target value approach.

For subjects who intend to undergo general surgery, gynaecological surgery and thoracic surgery assisted by the Thoracic and Abdominal Endoscopic Surgical System.

To use the Thoracic and Abdominal Endoscopic Surgical System developed by Shenzhen Cornerstone Robotics Technology Co., Ltd. to perform surgery in the above three disciplines, and to evaluate the efficacy and safety of the experimental medical device in the surgical treatment of the above three disciplines.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥ 18 and ≤ 80 years;
Body Mass Height Index (BMI) 18<BMI<30kg/㎡;
Patients identified by the investigator as suitable for general, gynaecological and thoracic surgery;
Written informed consent.

Exclusion criteria

Need for emergency surgery (e.g. gastric cancer, colorectal cancer combined with perforation, bleeding, obstruction, etc.);
With other malignancies or a previous history of other malignancies.
Preoperative imaging suggests that the tumour has distant metastases.
The patient has a history of relevant surgery or previous history of other malignancy and is judged by the investigator to be unsuitable for enrolment.
Severe bleeding tendencies or coagulopathic disorders.
With long-term use of anticoagulant and anti-platelet drugs (anti-platelet aggregation drugs discontinued less than 1 week prior to surgery), history of bleeding disorders or hematopoietic or coagulation disorders.
Significant immunodeficiency due to underlying illness (e.g. HIV/AIDS) and/or medication (e.g. systemic corticosteroids).
Women who are pregnant or nursing an infant.
With severe allergies and suspected or established alcohol, drug or substance addiction.
Other conditions which, in the opinion of the investigator, make participation in this trial inappropriate.