Gynecological disease
Conditions
Interventions
Trial group:At 12,24,36,48 and 72 hours after the operation, two groups of sticky electrodes were placed in the area of obvious shoulder pain. The treatment amount gently stimulated the skin according
Control group:Preoperative psychological care, health education
turnaround every 2 hours
analgesic medication according to postoperative pain.
Sponsors
Nanfang Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. All of patients were diagnosed as gynecological benign diseases: such as uterine fibroids, ovarian cysts, adenomyosis, ectopic pregnancy, etc., and with surgical indications, proposed to perform laparoscopic surgery; The 2. American Association of Anesthesiologists (ASA) grade is I-II; 3. Age 18 to 65 years old; 4. The patients volunteered to participate in this trial and signed an informed consent.
Exclusion criteria
Exclusion criteria: 1. The patient had a history of other induced shoulder pain, such as shoulder tuberculosis trauma; 2. Broken ulcer or infection occurred at the treatment site; 3. The patient has a high fever coma or is in the acute infection phase; 4. Patients have contraindications to electrical stimulation treatment, such as heart stent pacemaker and other medical stimulators; 5. Patients with cognitive communication or mental disorders; 6. Serious complications occurred during the surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative shoulder pain NRS scores; | — |
Secondary
| Measure | Time frame |
|---|---|
| Specific parts of shoulder pain;Body Mass Index;Length of stay;Postoperative comfort score was obtained;Postoperative anxiety scores;First exhaust time;Remediate the amount of analgesics;Operation duration;Time forthe first out of bed activities; | — |
Countries
China
Contacts
Public ContactSimeng Song
School of Nursing, Jinan University
Outcome results
None listed