CTRI/2018/06/014589招募中1 期
Efficacy and safety of intravenous paracetamol versus intramuscular tramadol hydrochloride as intrapartum analgesic: a randomised controlled study
government0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
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
入选标准
- •1. Primigravidae in spontaneous labour
- •2. Active phase of labour (cervical dilation of >=4cm,in the presence of adequate uterine 3 contractions per 10 minutes and each lasting at least for 40 seconds)
- •3. Maternal age between 18 to 35 years
- •4. Singleton term pregnancy(37 - 42 weeks of gestation)
- •5. vertex- presenting fetus
排除标准
- •1. clinical evidence of cephalopelvic disproportion
- •2. Malpresentation
- •3. scrred uterus , previous cesarean section, hysterotomy or myomectomy
- •4.medical disorders associated with pregnancy, especially severe anemia, jaundice, hypertension,diabetes, renal impairment
- •5. Fetal distress
- •6. Receiving any regional or parenteral analgesia before recuitment in the study.
- •7. Known hypersensitoivity to the drug family
- •8. induced labour
研究者
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