IRCT20220308054220N1尚未招募3 期
EFFICACY OF PARENTERAL ACETAMINOPHEN AS INTRAPARTUM ANALGESIC
Public sector medical college Rawalpindi Pakistan0 个研究点目标入组 130 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 130
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 35 years(—)
- 性别
- Female
入选标准
- •Primigravida of 18–35 year.
- •Full-term with uncomplicated spontaneous onset of labour at term (37–42 weeks gestation).
- •Singleton pregnancy.
- •Cervical dilatation of 3-5 cm.
- •Cephalic presentation of fetus.
排除标准
- •Malpresentation of fetus.
- •Multiparous women.
- •Previously scarred uterus (post myomectomy, post cesarean).
- •Preterm labour.
- •Antepartum hemorrhage.
- •History of drug allergy or hypersensitivity.
- •Fetal distress (abnormal foetal monitoring during labour).
- •Intrauterine foetal death.
- •Refusal by parturient.
- •History of alcohol/drug abuse.
- •Systemic and local sepsis.
- •Deranged coagulation profile.
- •Obstetric complications (e.g., premature rupture of amniotic membranes).
- •Women with clinical evidence of cephalopelvic disproportion.
研究者
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