TCTR20230530005招募中4 期
A Comparison of Two Low-Dose Regimens of Intravenous Fentanyl for Pain Relief during Labor: A Double Blinded, Randomized Controlled Trial
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 N/A (No limit)（—）
- 性别
- Female
入选标准
- •1. age 18 years or older
- •2. prefer not using an epidural
- •3. term pregnancy (37-42 weeks of gestation)
- •4. plan a vaginal birth
- •5. has a viable single fetus
- •6. with vertex presentation
- •7. no known psychological disorders
- •8. cervical dilatation of at 5-8 cm
- •9. visual analogue scale at least 4
排除标准
- •1. had received opioid such as pethidine or fentanyl within previous 24 hours
- •2. maternal respiratory rate less than 10 or maternal bradycardia (pulse rate less than 60) or oxygen saturation less than 95%
- •3. were diagnosed with conditions
- •(a)severe bronchial asthma
- •(b)Glaucoma
- •(c)heart or liver problems
- •(d)allergy or previous adverse reaction to opioids (such as fentanyl or pethidine)
- •(e)opioid substances dependency in last year
- •(f)taken antidepressants within the previous 14 days
- •(g)cognitive impairments or had an intellectual disability.
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