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临床试验/IRCT201307304969N8
IRCT201307304969N8已完成2 期

Comparison of the effect of prophylactic fibrinogen and placebo infusion on perioperative bleeding in posterior spinal fusion surgery, a randomized clinical trial

Iran University of Medical Sciences, Vice chancellor for research0 个研究点目标入组 42 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
42

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 60 years(—)
性别
All

入选标准

  • Patients candidate for elective posterior spine fusion surgery, preoperative serum fibrinogen level between 2-4 g/l, ASA I,II , age 18-60y, BMI less than 30 kg/m2, duration of surgery between 1-4 h,
  • Exclusion criteria: history of previous PSF, pulmonary, cardiac, hepatic, renal or coagulation disorders, hypertension, using beta blocker, calcium blocker, digoxine, TCAs, anticoagulant and clonidin by patient, alcohol or drug abuse, existing tumor in the site of surgery, surgery in more than 3 levels

排除标准

  • 未提供

研究者

发起方
Iran University of Medical Sciences, Vice chancellor for research

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