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临床试验/NCT02487303
NCT02487303已完成不适用

Intravenous Versus Oral Acetaminophen for Postoperative Pain Control After Cesarean Delivery

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 148 人开始时间: 2015年3月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
148
试验地点
1
主要终点
Cumulative Postoperative Opiate Consumption

研究概览

简要总结

This study will compare IV (intravenous) versus oral (PO) acetaminophen for postoperative pain after scheduled, elective Cesarean delivery. All patients will receive a standardized spinal anesthetic for operative anesthesia and will be randomized into one of three groups: (group 1) 1 gram IV acetaminophen every 8 hours for three doses, (group 2) 1 gram oral acetaminophen every 8 hours for three doses, or (group 3) no acetaminophen. This will be a randomized, open label study.

详细描述

This study will compare IV versus PO acetaminophen for postoperative pain in parturients after scheduled, elective Cesarean delivery. It is designed as a randomized, open label, controlled trial. All patients will receive a standardized spinal anesthetic for operative anesthesia and will be randomized into one of three groups: (group 1) 1 gram IV acetaminophen every 8 hours for three by a computer generated list.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Parturients 18 years
  • Elective Cesarean delivery
  • Spinal anesthesia
  • Able to consent to the study and participate in the follow-up.

排除标准

  • Weight under 50 kgs
  • Allergy to acetaminophen
  • General anesthesia
  • Urgent or emergent cases
  • Bleeding diathesis or other coagulopathy
  • G6PD deficiency
  • Liver disease
  • Substance abuse or dependence
  • HELLP syndrome
  • Thrombocytopenia or platelet dysfunction
  • History or active gastrointestinal bleeding
  • Acute kidney injury or chronic renal insufficiency
  • Contraindication/refusal to spinal anesthesia
  • Chronic pain
  • Chronic narcotic use
  • Illicit drug use
  • Allergy to any study related medications.

研究组 & 干预措施

Acetaminophen Oral

Active Comparator

(group 2) 1 gram oral acetaminophen every 8 hours for three doses

干预措施: Acetaminophen Oral (Drug)

Acetaminophen Intravenous

Active Comparator

(group 1) 1 gram IV acetaminophen every 8 hours for three doses

干预措施: Acetaminophen Intravenous (Drug)

结局指标

主要结局

Cumulative Postoperative Opiate Consumption

时间窗: 24 hours

Cumulative opiate consumption (IV morphine equivalents)

次要结局

  • Time to First Opiate Rescue(48 hours)
  • VAS (Visual Analog Scale)(24 hours)
  • Time Discharge(24 hours postoperative)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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