About this trial
In this study, a prospective study is used to select patients who will undergo intra-abdominal endoscopic single-port surgery system for benign gynecological diseases from February 2025 to December 2026 in the Second Affiliated Hospital of Wenzhou Medical University, including hysterectomy, myomectomy, ovarian cyst removal and adnexectomy. The study will perform statistical analysis to evaluate the feasibility and the main factors affecting the safety of intra-abdominal endoscopic single-port surgery system(SR-ENS-600) used in gynecological day surgery.
Eligibility criteria
Qualifiers
Women aged 18 to 75 years old, with a body mass index (BMI) of no more than 32 kg/m2;
Conscious, no history of mental illness, accompanied by an adult during the perioperative period;
Educate the subjects, who are willing to undergo day surgery, understand and accept the surgical method and anesthesia method;
Subjects and families understand perioperative care and are willing and able to complete post-discharge care;
Disqualifiers
Moderate and high-risk patients will be excluded based on ANGEL adhesion risk scoring system;
Subjects with hemorrhagic rupture of ectopic pregnancy and unstable vital signs;
Genital tract infection or in the acute phase of systemic infection;
Subjects on long-term anticoagulant therapy or with coagulation dysfunction;
Trial design
Treatments tested in this trial
- Domestic single-port laparoscopic surgery system