The CAPTAIN Trial: Cerebrolysin Asian Pacific Trial in Acute Brain Injury and Neurorecovery

Last updated: February 24, 2020
Sponsor: Ever Neuro Pharma GmbH
Overall Status: Terminated

Phase

4

Condition

Traumatic Brain Injury

Memory Loss

Neurologic Disorders

Treatment

N/A

Clinical Study ID

NCT01606111
EVE-CN-0610
  • Ages 18-60
  • All Genders

Study Summary

The purpose of this trial is to investigate safety and efficacy of Cerebrolysin as add-on therapy to standard care in patients with acute traumatic brain injury (TBI). The study duration for each patient is 180 days.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Clinical diagnosis of TBI and a GCS 7-12

  • Only isolated TBI

  • CT

  • Pre-Trauma Karnofsky-Index = 100

  • Age 18-60 years

  • Male and female patients

  • Time to needle for study medication within 6 hours after injury

  • Patient is not pregnant or lactating during the trial and is not of childbearingpotential

  • Patient was able to speak, read and write in a pre-defined study language before theaccident.

  • Reasonable expectation of completion of outcome measures at follow-up

  • Written informed consent

Exclusion

Exclusion Criteria:

  • Evidence of pre-existing major health problems

  • Any neurological or non-neurological condition independent from TBI that mightinfluence the functional outcome or other efficacy outcome measures

  • Injury of writing hand influencing cognitive or other outcome measures

  • Clear clinical signs of intoxication influencing the evaluation

  • Major drug dependency including alcohol

  • Chronic treatment with steroids, Ca2+-channel blockers or major anticoagulants

  • Penetrating high-velocity missile head trauma

  • Stab wound trauma into the brain

  • Patients with spinal cord injury

Study Design

Total Participants: 46
Study Start date:
September 01, 2013
Estimated Completion Date:
July 31, 2015

Connect with a study center

  • Prince of Wales Hospital

    Hong Kong,
    Hong Kong

    Site Not Available

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