跳至主要内容
临床试验/jRCTs042230072
jRCTs042230072进行中(未招募)不适用

Feasibility and safety study of PuraStat (a novel self-assembling peptide) for exudative hemorrhage after stapling of pulmonary artery during thoracic surgery

未提供0 个研究点目标入组 21 人开始时间: 2023年9月14日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
21
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
18age old over 至 No limit(—)
性别
All

入选标准

  • (1) Age 18 years or older
  • (2) ECOG performance status (PS) is 0 or 1
  • (3) Planned surgery is scheduled within 2 weeks
  • (4) Patient is scheduled for an anatomical lung resection (segmentectomy, lobectomy, bilobectomy, pneumonectomy or a combination of these surgical procedures)
  • (5) Major organ function is preserved
  • (6) Written informed consent has been obtained

排除标准

  • (1) Patients with a history of coagulation disorder
  • (2) Patients with psychiatric disorders that make it difficult to include in the study
  • (3) Patients receiving continuous systemic administration of steroids or immunosuppressants
  • (4) Patients with a history of hypersensitivity to peptide or protein products
  • (5) Patients with a history of serious hypersensitivity

结局指标

主要结局

-

Rate of additional hemostatic treatment required

次要结局

未报告次要终点

研究者

发起方
未提供

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