Labor analgesia \ cesarean section
Conditions
Interventions
experimental group:Dexmedetomidine
control group:Normal saline
Sponsors
Tianjin Central obstetrics and Gynecology Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1. ASA class I-II, 20-35-year-old primipara, 38-41 weeks of gestation; 2. The primipara who transferred to caesarean section midway through epidural labor analgesia; 3. Patients without previous abdominal and perineal operation history; 4. Patients with epidural labor analgesia.
Exclusion criteria
Exclusion criteria: 1. Patients who can't perform epidural block in emergency cesarean section; 2. Patients with Epidural Delivery Analgesia catheter prolapse; 3. Patients with gestational hypertension, heart disease, morbid obesity and diabetes (including gestational diabetes); 4. Patients who are allergic to local anesthetics and opioids; 5. Patients with pain relief time more than 24 hours.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Failure rate of epidural anesthesia; | — |
Secondary
| Measure | Time frame |
|---|---|
| Ramsay Sedation score;Catecholamine concentration;The visual analog scales; | — |
Countries
China
Contacts
Public ContactPeijun Zhang
Tianjin Central Obstetrics and Gynecology Hospital
Outcome results
None listed