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临床试验/NCT02229968
NCT02229968进行中(未招募)2 期

Efficacy of ε-Aminocaproic Acid (EACA) in Children Undergoing Craniofacial Reconstruction Surgery

Children's National Research Institute1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2014年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
22
试验地点
1
主要终点
Intraoperative blood loss

研究概览

简要总结

The purpose of this study is to determine whether Amicar (ε-aminocaproic acid) is effective in reducing blood loss in children undergoing craniofacial reconstruction surgery.

The investigators hypothesize that Amicar will decrease intraoperative blood loss and decrease the need for perioperative blood product administration in children undergoing craniofacial surgery.

详细描述

Craniosynostosis is a condition in which there is premature fusion of one or more of the sutures between the bones of the skull. Premature fusion of sutures in the skull limits the ability of the cranial vault to expand to accommodate the rapidly growing brain in infancy and early childhood and leads to bony deformation. Left uncorrected, craniosynostosis may adversely impact both neurologic and psychosocial development and in some cases, can result in high intracranial pressure and blindness.

Craniofacial (CF) reconstructive surgery is performed in young children with craniosynostosis to improve physical appearance, prevent functional neurologic disturbances, and enhance psychosocial development. Due to the complexities of the surgery as well as the young age and size of the patients, CF reconstruction carries potential life threatening risks and can result in significant morbidity. Reported complications include massive intraoperative hemorrhage, intraoperative cardiac arrest, transfusion-related reactions, venous air embolism, hypotension, coagulopathy, bradycardia, postoperative seizures, surgical site infections, facial swelling with airway compromise, and unplanned postoperative mechanical ventilation. The most severe and most common perioperative issues relate to the rate and extent of blood loss.

Fibrinolysis, which impairs adequate hemostasis, has been shown to occur in children during CF reconstruction. This most certainly contributes to the magnitude of blood loss in these types of operations. Thus, targeting this defect in clot hemostasis with the use of antifibrinolytics is a reasonable therapeutic approach.

Amicar (ε-aminocaproic acid) is a synthetic lysine analog that blocks the lysine binding sites on plasminogen, resulting in antifibrinolytic activity through inhibition of plasmin formation. We have chosen to study Amicar in this clinical context for a number of reasons. First, major hemorrhage continues to be a significant perioperative issue in this cohort. Secondly, Amicar is commonly and safely administered to children undergoing other types of high-risk surgery (i.e., spinal fusion surgery and open heart surgery). In addition, Amicar is inexpensive and easily administered, making it a viable and novel therapeutic option if shown to be effective for this type of surgery.

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
2 Months 至 36 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Any child diagnosed with craniosynostosis in need of surgical repair
  • Males and females between the ages of 2 - 36 months (minorities will be included)
  • Surgical procedure involving complex craniofacial reconstruction and craniotomy
  • Written informed consent from parent/guardian

排除标准

  • Subjects with known or suspected hypersensitivity reaction to Amicar or history of prior Amicar exposure
  • Presence or prior history of a known coagulation disorder or hypercoagulable state
  • Preoperative laboratory values that indicate clinically significant hematologic disease (hemoglobin, platelet count, prothrombin time, or partial thromboplastin time outside of normal range)
  • Subjects who are on anticoagulant therapy (Coumadin, heparin, aspirin, etc.)
  • Subjects with a prior history of a thrombotic event
  • History of renal malformation
  • Presence of hematuria
  • History of abnormal renal function - serum creatinine or blood urea nitrogen (BUN) value greater than 1.5 times the upper limit of the normal range
  • Craniofacial reconstruction surgery performed in conjunction with an additional surgical procedure associated with blood loss
  • Subjects who have been previously enrolled in this protocol may not be enrolled again

研究组 & 干预措施

normal saline

Placebo Comparator

Treatment group 2: Equal volume of normal saline (placebo control) at the same rate as treatment group 1.

干预措施: normal saline (Drug)

Amicar (ε-aminocaproic acid)

Experimental

Treatment group 1: Amicar 100 mg/kg (0.4 mL/kg) IV loading dose, followed by an intraoperative continuous infusion at 40 mg/kg/hr (0.16 mL/kg/hr) to be continued until skin closure.

干预措施: Amicar (ε-aminocaproic acid) (Drug)

结局指标

主要结局

Intraoperative blood loss

时间窗: within the first 72 hours after surgery

As estimated blood loss is known to be inaccurate in this setting, mean intraoperative blood loss (in mL/kg) will be calculated using a formula previously described in this population.

次要结局

  • Blood donor exposure(within the first 30 days after surgery)

研究者

发起方
Children's National Research Institute
申办方类型
Other
责任方
Sponsor

研究点 (1)

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