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临床试验/NCT04766281
NCT04766281招募中4 期

Safety and Efficacy of MLC901 (NeuroAiD Ii) in Patients With Moderate TBI: A Randomized Double Blind Placebo Controlled Trial

University of the Philippines5 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2021年5月1日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
120
试验地点
5
主要终点
GOS-E at 6 months

研究概览

简要总结

This study wants to evaluate whether MLC901 will help improve the condition of adult patients with moderate traumatic brain injury.

详细描述

This is a double blind placebo controlled randomized trial to determine whether giving MLC901 for 6 months will improve the outcomes in a adult patients with moderate traumatic brain injury.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-65 years
  • Moderate TBI
  • Presenting at the study site within 7 days of injury
  • Participant or his/her legal representative able to comply with the study protocol and willing to provide written informed consent

排除标准

  • Penetrating HI
  • Co-existing severe or unstable injury
  • Physician's medical judgment that surgical intervention is likely within the next 48 hours
  • Physician's medical judgment that participation is not in the participant's best interest
  • Pre-injury mRS>2
  • Pregnancy
  • Inability to take study drug orally or via NGT
  • Participation in another investigational drug study
  • Intake of nootropic drugs which are not standard TBI medications

结局指标

主要结局

GOS-E at 6 months

时间窗: 18 months

This is the most widely used TBI outcome measure with the extended version ranging from 0 (dead) to 8 (full recovery)

次要结局

  • Safety until 9 months: adverse events(18 months)
  • Glasgow Coma Scale (GCS) at baseline, 1, 3, 6 & 9 months(18 months)
  • Frontal Assessment Battery at 1,3,6 & 9 monts(18 months)
  • EQ-5D at 1,3,6 & 9 months (EuroQol Group)(18 months)
  • Glasgow Outcome Scale Extended (GOS-E) at baseline, 1,3 & 9 months(18 months)
  • Mortality at 6 months(18 months)
  • Montreal Cognitive Assessment Filipino Version (MoCA-P) at 1,3,6 & 9 months(18 months)
  • RiverMead Postconcussion Symptome Questionnaire Score at 1,3,6 & 9 months(18 months)
  • Compliance until 6 months(18 months)
  • Cerebral swelling at baseline, 1 & 2 weeks(18 months)
  • Barthel Index (BI) at 1,3,6 & 9 months(18 months)
  • Hospital Anxiety and Depression Scale at 1,3,6 & 9 months(18 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Annabell Chua

Principal Investigator

University of the Philippines

研究点 (5)

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