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临床试验/TCTR20230105001
TCTR20230105001已完成不适用

Comparing intraoperative opioid consumption in patients who received preemptive oral paracetamol versus no preemptive oral paracetamol in elective cranial surgery.

/A0 个研究点目标入组 336 人开始时间: 2023年1月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
336

研究概览

简要总结

Preemptive oral paracetamol before elective cranial surgery reduces intraoperative fentanyl consumption by 5.1 mcg/hr (p- value 0.02, 95% CI 0.8 to 9.3).

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 90 Years(—)
性别
All

入选标准

  • 1.Elective cranial surgery patients including craniotomy and craniectomy surgery
  • 2.Age 18-90 years
  • 3.ASA class I-III

排除标准

  • 1. Emergency surgery
  • 2. Awake craniotomy
  • 3. Age less than 18 years
  • 4. Use of intraoperative IV paracetamol without preemptive oral paracetamol
  • 5. Use of intraoperative IV lidocaine
  • 6. Use of IV opioid infusion intraoperatively
  • 7. Use of preoperative pain medications
  • 8. Cranial biopsy
  • 9. Transsphenoidal surgery
  • 10. Cranioplasty surgery
  • 11. Pregnant Patients

研究者

发起方
/A

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