跳至主要内容
临床试验/EUCTR2009-012338-56-AT
EUCTR2009-012338-56-AT进行中(未招募)不适用

AN EXPLORATIVE PHASE IIa STUDY TO ASSESS SAFETY, TOLERABILITY,PHARMACODYNAMICS AND PHARMACOKINETICS OF VAS203 IN PATIENTS WITHMODERATE AND SEVERE TRAUMATIC BRAIN INJURY - NOSTRA TRIA

vasopharm GmbH0 个研究点目标入组 32 人开始时间: 2011年1月12日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
32

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Written informed consent from patient’s legal guardian or legal representative,
  • according to local requirements
  • 2. 18 - 65 years of age, inclusive
  • 3. Head trauma within the last 12 hours
  • 4. TBI with Glasgow Coma Score (GCS) = 3 and that requires Intracranial pressure
  • (ICP) monitoring.
  • 5. Catheter placement (intraventricular or intraparenchymal only) for monitoring and
  • management of increased ICP
  • 6. Microdialysis probe placement in predominantly injured hemisphere ipsilateral to contusion if focal
  • (evaluated by computer tomography [CT])
  • 7. Systolic blood pressure = 100 mmHg
  • 8. Females of child-bearing potential must have a negative pregnancy test
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Penetrating head injury (e.g. missile, stab wound)
  • 2. Not expected to survive more than 24 hours after admission
  • 3. Concurrent, but not pre-existing, spinal cord injury
  • 4. Unilateral and bilateral fixed and dilated pupil (> 4 mm)
  • 5. Cardiopulmonary resuscitation performed post injury, or extracranial injuries causing continuing bleeding likely to require multiple transfusions (> 4 units red blood cells)
  • 6. Coma due to a pure” epidural hematoma (lucid interval and absence of structural
  • brain damage on CT scan)
  • 7. Coma suspected to be primarily due to other causes than head injury (e.g. drug
  • overdose, alcohol intoxication, drowning/near drowning)
  • 8. Known or CT scan evidence of pre-existing major cerebral damage
  • 9. Decompressive craniectomy, planned prior to randomisation/enrolment
  • 10. Polytraumatic patients with Injury Severity Score non head > 18
  • 11. Rhabdomyolysis with CK > 5000 IU/L
  • 12. Injuries to ascending aorta and/or carotid arteries and/or vertebral arteries.
  • 13. Serum creatinine values > 1.5 mg/dL (133 µmol/L)
  • 14. Estimated glomerular filtration rate (eGFR) < 60 ml/min by Modification of Diet in
  • Renal Disease (MDRD) formula
  • 15. Body mass index (BMI) < 19 kg/m2 and > 35 kg/m2, Body weight < 50 kg and > 120 kg.
  • 16. Any severe concomitant condition (cancer; haematologic, renal, hepatic, coronary
  • disease; major psychiatric disorder; alcohol or drug abuse), that can be ascertained at admission
  • 17. Known to have received an experimental drug within 4 weeks prior to current injury
  • 18. Administration of > 100 ml of contrast media containing iodine

研究者

相似试验

进行中(未招募)
不适用
AN EXPLORATIVE PHASE IIa STUDY TO ASSESS SAFETY, TOLERABILITY,PHARMACODYNAMICS AND PHARMACOKINETICS OF VAS203 IN PATIENTS WITHMODERATE AND SEVERE TRAUMATIC BRAIN INJURY - NOSTRA TRIA
EUCTR2009-012338-56-GBvasopharm GmbH32
进行中(未招募)
1 期
AN EXPLORATIVE PHASE IIa STUDY TO ASSESS SAFETY, TOLERABILITY,PHARMACODYNAMICS AND PHARMACOKINETICS OF VAS203 IN PATIENTS WITHMODERATE AND SEVERE TRAUMATIC BRAIN INJURYModerate to severe traumatic brain injuryMedDRA version: 9.1Level: LLTClassification code 10060690Term: Traumatic brain injury
EUCTR2009-012338-56-FRvasopharm GmbH32
进行中(未招募)
1 期
This is an open-label, Phase 2, exploratory study to examine the safety and efficacy of inarigivir in non-cirrhotic, hepatitis B e antigen (HBeAg)-negative subjects with chronic hepatitis B virus (HBV) infection.Chronic HBV-infected, HBeAg-negative subjects, who are non-cirrhotic and meet the cohort-specific criteria. Criteria for the planned cohorts are as follows:Cohort 1 Subjects who have been on NUC treatment for =3 years, have HBsAg <1000 IU at Baseline, and are planning to discontinue NUC therapyCohort 2 Subjects who have been suppressed on a NUC for =1 year, and have HBV DNA below LLOQ, and are planning to continue NUC therapy
EUCTR2019-000896-17-GBSpring Bank Pharmaceuticals, Inc.60
招募中
1 期
XT007_Hemophilia-A_NXT001JG (NXTAGE)Hemophilia A
JPRN-jRCT2080224835Chugai Pharmaceutical Co., Ltd.106
进行中(未招募)
1 期
A Study to Assess Safety, Effectiveness, Pharmacokinetics, and Pharmacodynamics of RO7112689 in Healthy Volunteers and Patients with Paroxysmal Nocturnal HemoglobinuriaParoxysmal nocturnal hemoglobinuria (PNH)MedDRA version: 21.1Level: LLTClassification code: 10055629Term: Paroxysmal nocturnal hemoglobinuria Class: 10038359
CTIS2023-506287-14-00F. Hoffmann-La Roche AG32