Benign gynecological diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) The age ranged from 18 to 60 years; 2) Women with sexual life history; 3) Patients with benign gynecological diseases need surgical treatment; 4) The vital signs are stable and can tolerate endoscopic surgery; 5) Patients were able to understand the protocol and willing to participate in the study, and provided written informed consent.
Exclusion criteria
Exclusion criteria: 1) Pregnant women; 2) The diameter of adnexal mass was larger than 8-10 cm, the uterine enlargement was larger than that of 3-month pregnancy; 3) Patients with previous history of pelvic inflammatory disease and pelvic adhesion; 4) Patients with pelvic endometriosis; 5) There was a history of multiple pelvic and abdominal surgery (cesarean section more than 2 times); 6) Patients with vaginitis symptoms or without improvement after treatment; 7) Patients with palpable or suspicious uterine rectal fossa closure, nodule or scar, and vaginal stenosis; 8) The presence of mental illness or drug abuse that may affect compliance with the trial requirements is known;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Operation time;Anesthesia time;volum of bleeding during operation;Operative complications;Postoperative pain score;The time of first sexual intercourse after operation;Sexual satisfaction;Inflammatory cytokines and immune factors, etc; | — |
Secondary
| Measure | Time frame |
|---|---|
| The use of analgesics;Exsufflation time after operation;The time of urination and defecation was restored after operation;The time of getting out of bed for the first time after operation;Postoperative nausea / vomiting;Satisfaction of postoperative quality of life;Length of stay;Hospitalization expenses;Wound recovery 1 month after operation; | — |
Countries
China
Contacts
Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China