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临床试验/NCT00371215
NCT00371215已完成2 期

A Phase 2 Study of Recombinant Human Thrombin (rThrombin) Administered Using a Spray Applicator in Subjects Undergoing Autologous Skin Grafting Following Burn or Traumatic Skin Injury

ZymoGenetics1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2006年8月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
ZymoGenetics
入组人数
72
试验地点
1
主要终点
The incidence and severity of adverse events

研究概览

简要总结

The purpose of this study is to evaluate whether rThrombin is safe when used for controlling bleeding during skin graft surgery.

详细描述

This is a Phase 2 multiple site, single-arm, open-label study designed to evaluate the safety of rThrombin in subjects of age 2 to 75 years who are receiving a partial- or full-thickness autologous sheet or mesh grafts following burn or traumatic skin injury. After establishing eligibility, study participants will be treated with topical spray rThrombin at the skin graft recipient site during autologous skin graft surgery. There will be a 1-month follow-up period after the surgery.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Autologous skin grafting with sheet or mesh grafts following burn or traumatic skin injury

排除标准

  • Known antibodies or hypersensitivity to thrombin or other coagulation factors

研究组 & 干预措施

1

Experimental

rThrombin

干预措施: rThrombin (Biological)

结局指标

主要结局

The incidence and severity of adverse events

时间窗: Up to day 29

次要结局

  • The incidence and grade of clinical laboratory abnormalities(Up to day 29)
  • The incidence of anti-rThrombin product antibodies(Up to day 29)
  • The incidence of hemostasis(Up to 20 minutes)
  • The percentage of graft take(Up to day 29)
  • The incidence of re-grafting(Up to day 29)

研究者

发起方
ZymoGenetics
申办方类型
Industry

研究点 (1)

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