Clinical study of dexmedetomidine for analgesia in epidural delivery
Not Applicable
Recruiting
- Conditions
- NA
- Registration Number
- ChiCTR2400088860
- Lead Sponsor
- Shanghai 10th People's Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
- Full term primiparous expectant mothers;<br>2. Age 20-35 years old;<br>3. Fetal absence of complications such as intrauterine distress, amniotic fluid contamination, cephalopelvic imbalance, and intrauterine infection;<br>4. All sign informed consent forms;<br>5. Willing to follow research requirements
Exclusion Criteria
- Pregnant women with concomitant mental illness, cardiovascular and other important organ diseases;<br>2. Pregnant women without postoperative pain relief requirements;<br>3. There are contraindications for spinal anesthesia;<br>4. Opioid drug addicts;<br>5. Pregnant women with abnormal fetal heart rate monitoring (fetal heart rate>160 beats/minute or<120 beats/minute, lasting for 10 minutes)
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score;
- Secondary Outcome Measures
Name Time Method body temperature;epidural anesthesia block level;Improved Bromage rating;blood pressure;heart rate;Rate of vaginal delivery to cesarean section;Duration of the first stage of labor;Second stage of labor duration;Duration of the third stage of labor;The analgesic duration;Neonatal Apgar score;Perceived blockade score;Adverse reactions;