Gynecological perioperative pain
Conditions
Interventions
control group:Routine postoperative care, and administration of analgetic and antibiotics
experimental group:Routine postoperative care+ Virtual reality (VR) therapy
Sponsors
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Eligibility
Sex/Gender
Female
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: (1) Non-pregnant women, aged 18-70 years, who were admitted to hospital for benign gynecological diseases and intended to undergo hysteroscopic, laparoscopic or combined surgery; (2) Patients are willing to participate in this study; (3) Have certain reading ability and can complete the questionnaire independently.
Exclusion criteria
Exclusion criteria: (1) Suspected malignant tumor before surgery, known anatomical abnormalities that may make surgery difficult before surgery; (2) Combined with serious other systemic diseases, including motion sickness, claustrophobia, etc.; (3) Patients with hearing and visual impairment; (4) Patients unable to cooperate with the questionnaire due to language and cultural level; (5) pregnant patients; (6) Unwilling to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain level 7 hours after surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain and anxiety at 6 hours after surgery;Anxiety level 7 hours after surgery;Degree of dizziness, nausea, vomiting, and diarrhea 6 hours after surgery;Degree of dizziness, nausea, vomiting, and diarrhea 7 hours after surgery;Maximum postoperative pain level;Patient tolerance;Age;Menopausal state;Whether to deliver or not;Number of previous operations;Total length of stay;Total hospitalization costs; | — |
Countries
China
Contacts
Public ContactLong Tengfei
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Outcome results
None listed