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临床试验/NCT00242437
NCT00242437已完成4 期

A Prospective, Multicenter Study to Evaluate Hemostatic Matrix With Bovine Thrombin in Achieving Hemostasis in Patients Undergoing Endoscopic Sinus Surgery

Ethicon, Inc.6 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2005年10月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
Ethicon, Inc.
入组人数
30
试验地点
6
主要终点
Success in achieving hemostasis after product application

研究概览

简要总结

Evaluating clinical performance of Hemostatic Matrix with bovine thrombin in achieving hemostasis in patients undergoing endoscopic sinus 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
Ect
盲法
None

入排标准

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

入选标准

  • Patients who are 18 years or older.
  • Patients undergoing elective primary or re-do endoscopic sinus surgery for chronic sinusitis with bleeding surface requiring an adjunct to achieve hemostasis.
  • Patients must be willing and capable of cooperating to the extent and degree required by the protocol and sign the IRB approved Informed Consent Form prior to any participation in the study.

排除标准

  • Patients with bleeding diathesis, pathologic coagulopathy, systemic disorders, inflammatory conditions (other than chronic sinusitis or nasal polyposis) or autoimmune, immunodeficiency diseases or any other disorder that may interfere with hemostasis.
  • Patients with severe (brisk or forceful) bleeding site(s).
  • Patients undergoing urgent or emergency endoscopic sinus surgery.
  • Patients with bronchial asthma who have aspirin intolerance.
  • Patients with diffuse polyposis that would require chronic oral steroids or patients on chemotherapeutic agents that might delay healing (short term pulse steroid therapy and topical steroids are acceptable).
  • Patients who have used anticoagulant, antiplatelet or nonsteroidal anti-inflammatory analgesic (NSAID) within 7 days prior to surgery.
  • Patients who are morbidly obese (Body Mass Index > 35).
  • Patients with acute local infection at the operative side.
  • Patients who are current alcohol and/or drug abusers.
  • Patients with neoplasm, craniofacial abnormalities (e.g. cleft palate), or sleep apnea using nasal CPAP, or patients that may require a Lothrop procedure.
  • Female patients who are pregnant or nursing.
  • Patients who have uncontrolled diabetes mellitus (blood glucose levels >400 mg/dl) as determined by the Investigator based on medical history.
  • Patients who have participated in another investigational drug or device research within 30 days of enrollment.
  • Patients with known antibodies to bovine thrombin preparations, sensitivities or religious prohibitions to porcine gelatin or bovine components.

结局指标

主要结局

Success in achieving hemostasis after product application

次要结局

  • Post operative healing
  • Patient Satisfaction
  • Time to hemostasis

研究者

发起方
Ethicon, Inc.
申办方类型
Industry

研究点 (6)

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