Iv controlled analgesia after cesarean section
Conditions
Interventions
Experimental group:Dexmedetomidine + sufentanil
Sponsors
Nanchong Central Hospital of Sichuan Province
Eligibility
Sex/Gender
Female
Age
20 Years to 42 Years
Inclusion criteria
Inclusion criteria: 1. Subjects aged 20-42 years; 2. ASA grade: I-II; 3. Primipara with single birth at 37-40 weeks of gestation; 4. The first set of doctors in the same group underwent elective cesarean section on the same day; 5. Subjects willing to breastfeed.
Exclusion criteria
Exclusion criteria: 1. Subjects allergic to adrenergic agonists and opioids; 2. There were subjects who often used analgesics and sedatives before operation; 3. Subjects with previous psychiatric history, spinal and lower abdominal surgery history; 4. Subjects sensitive to pain; 5. Subjects with conduction block and sinus bradycardia on ECG before operation; 6. Those who can't understand pain score and those who don't know how to use PCIA; 7. Subjects who have participated in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score;Sufentanil dosage; | — |
Countries
China
Contacts
Public ContactWuchang Fu
Nanchong Central Hospital of Sichuan Province
Outcome results
None listed