Gynecology
Conditions
Interventions
A :V-NOTES
B :porous laparoscope
Sponsors
Chengdu Women's and Children's Center Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1)Subjects volunteered to join the study and signed informed consent; 2) Female patients aged 18-60 with a history of sexual life and without pregnanc; 3) Researchers believe that subjects can comply with the research plan; 4) Preoperative examination revealed benign and surgically indicated accessory disease.
Exclusion criteria
Exclusion criteria: 1)Participated in other clinical trials within 3 months before participating in this clinical trial; 2)Patients with severe underlying diseases who cannot tolerate surgical anesthesia; 3)Past pelvic and abdominal surgery more than 2 times; 4) Vaginal inflammation or no improvement after treatment; 5) Estimate of patients with severe adhesion within accessory area; 6) Active infections of other organs; 7)Mental illness or drug abuse known to have an impact on compliance with test requirement; 8)Human immunodeficiency virus (HIV) infection; 9)Other circumstances that the researchers consider unsuitable for this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| operation time;Surgical bleeding volume;Postoperative anal exhaust time;Postoperative urinary catheter time;Postoperative bedtime;Postoperative pain grading;Comparison of surgical costs;Quality of life;KPS score; | — |
Countries
China
Contacts
Public ContactChen.Ying
Chengdu Women's and Children's Center Hospital
Outcome results
None listed