A randomized controlled study for acupoint stimulation using subacupuncture to relieve postoperative nausea and vomiting in patients undergoing gynecological and obstetrical surgery
Phase 1
- Conditions
- ausea and vomiting
- Registration Number
- ITMCTR1900002678
- Lead Sponsor
- Hebei Hospital of Traditional Chinese Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
1. Patients who planned gynecological surgery and cesarean section;
2. Non-smoker;
3. Patients with a history of motion sickness;
4. Opioid patients;
5, Aged > 18 years and < 65 years;
6, ASA class I - II.
Exclusion Criteria
1. Patients who refuse acupoint stimulation;
2. Patients with antiemetic drugs;
3. Patients with dexamethasone;
4, mental disorders, unable to communicate with patients;
5. Allergic to adhesive tape and hypodermic acupuncture.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of nausea and vomiting;
- Secondary Outcome Measures
Name Time Method