Upper abdominal pain after laparoscopic surgery Surgery
Conditions
Interventions
Participants are randomly assigned to the experimental group and control group, four hours after the operation. Randomisation uses a random number table.
The experimental group starts
Sponsors
Chung Shan Medical University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Those gynecological patients who have undergone laparoscopic surgery 2. Adults over 20 years old 3. A clear consciousness can speak, read and understand Mandarin. And those who can fully cooperate 4. Those who accept this experiment and sign the consent form. 5. Those who take general anesthesia 6. If the experimental group and the control group are in the same ward, at least one ward will be separated 7. The attending physician agrees
Exclusion criteria
Exclusion criteria: 1. Failed laparoscopic surgery was changed to laparotomy 2. Those who have had a shoulder injury 3. BMI value> 30mg/m² 4. Mental patients who are unable to cooperate in the implementation of intervention measures 5. The experimental group and the control group are allocated by random assignment. If the experimental group and the control group are allocated to the same ward, the second income patient will be excluded. Avoid cross-effects and violate research ethics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain is measured used a visual analogue scale at 4 hours and 24 hours after operation | — |
Secondary
| Measure | Time frame |
|---|---|
| Recovery from surgery is measured QoR-40 questionnaire at 4 hours and 24 hours after operation | — |
Countries
Taiwan
Outcome results
None listed