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.
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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Surgery with the Cornerstone Surgical Robot.
Sir Run Run Shaw Hospital Affiliated to Zhejiang University School of Medicine
Hangzhou, Zhejiang, China
Surgical non-referral rate
Surgical untransferred is defined as not converted from an experimental medical device assisted method to another surgical device control system assisted, laparoscopic surgery or open surgery.
Time frame: during the surgery
The surgeon's operating time
Operative time(minutes)
Time frame: during the surgery
Length of postoperative stay
Total number of days the patient was in hospital from the day of surgery to discharge.
Time frame: up to 12 weeks
Intraoperative blood loss
Estimated blood loss(milliliters,ml)
Time frame: during the surgery
Length of stay
The postoperative day when patients complied with the predefined discharge criteria
Time frame: The patient's total number of days from the day of surgery to discharge was recorded 30 days postoperatively.
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