Propofol injection pain
Conditions
Interventions
Sponsors
Department of Anesthesiology, the First Affiliated Hospital of Wenzhou Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Women aged 18 to 65 years who were selected for painless hysteroscopy; 2. ASA grade I-II; 3. BMI kg/m2 18-31; 4. No contraindication of propofol and lidocaine; 5. informed consent to this pre-treatment programme.
Exclusion criteria
Exclusion criteria: 1. meridian points have surgical incision or scar; 2. patients with local skin infection at acupoints; 3. patients with upper or lower limb nerve damage; 4. have a history of spinal surgery; 5. other clinical trials in the last four weeks; 6. can't understand NRS score; 7. patients with history of allergy to lipids, propofol, local anesthetics (lidocaine) and general anesthesia; 8. patients with forearm thrombophlebitis or acute and chronic pain syndrome; 9. has a history of gastrointestinal ulcers and analgesic and sedative drug abuse; 10. Severe mental illness or Patients with dyslexia; 11. Patients with chronic pain syndrome, thrombophlebitis, neurological disorders; 12. The researchers found it inappropriate to participate in the trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS; | — |
Countries
China
Contacts
Public ContactMo Yunchang
Department of Anesthesiology, The First Affiliated Hospital of Wenzhou Medical University
Outcome results
None listed