Uterine fibroids
Conditions
Interventions
Sponsors
Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1) 18~65 years old 2) With or without clinical symptoms 3) Color Doppler ultrasound suggests uterine fibroids, single or multiple, with a diameter of 5~12cm 4) Gynecological examination, the uterus is larger than 2+months of pregnancy 5) American Association of Anesthesiologists (A) Grade 1-11; 6) Patients who are willing to choose day surgery 7) Patients can understand the program and are willing to participate in the study, and provide written informed consent
Exclusion criteria
Exclusion criteria: 1) Body temperature > 37.4 degrees C; 2) Hb < 80g/L; 3) Color Doppler ultrasound suggests submucosal uterine fibroids; 4) Highly suspected malignant tumors; 5) With internal and surgical complications such as hypertension, diabetes, heart disease, etc., it is not effective Controlled; 6) Acute genital tract inflammation; 7) Multiple abdominal surgery history, severe pelvic adhesions; 8) Participated in other clinical trials within three months before participating in this experiment; 9) There is already a possibility of compliance with the requirements of this experiment Circumstances of affected mental illness or drug abuse; 10) Circumstances deemed unsuitable for participating in this clinical trial by other researchers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Operation time;Intraoperative blood loss;Perioperative complications;Whether to transfer to porous laparoscopy or open surgery;Time to get out of bed for the first time after surgery;Whether to transfer to the general ward;First exhaust time after operation;Whether to return to surgery unplanned;Time of first meal after operation;visual analoge scale score for postoperative pain;visual analoge scale score for postoperative pain;Whether to delay discharge;Rehospitalization rate 30 days after surgery;Patient satisfaction; | — |
Secondary
| Measure | Time frame |
|---|---|
| patient's life quality scale;Hospital costs; | — |
Countries
China
Contacts
Public ContactXiao-Qin Gan
Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Outcome results
None listed