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Efficacy and Safety of Rivastigmine in Patients With Traumatic Brain Injury and Cognitive Impairment

Primary Purpose

Traumatic Brain Injury

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Rivastigmine
Sponsored by
Novartis
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury focused on measuring Traumatic brain injury,, cognitive impairment,, rivastigmine

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All Sexes

Inclusion Criteria: Traumatic brain injury confirmed by available brain imaging (CT or MRI) and be at least 52 weeks post injury Neuropsychologic disturbances indicated by: impaired memory (reduction of below 1 standard deviation (SD) of the mean on the California Verbal Learning Test (CVLT) and impaired executive function (reduction of below 1 standard deviation (SD) of the mean on the Verbal Memory Learning Test (VLMT) and Tower of London Test (ToL) and impaired attention (reduction of below 1 standard deviation (SD) of the mean on the Test Battery for Attentional Performance (TAP) Be required to have had sufficient education to read, write, and effectively communicate Be cooperative, able to ingest oral medication, and able to complete all aspects of the study and capable of doing so, either alone or with the aid of a responsible caregiver according to the investigator's judgement Exclusion Criteria: A current diagnosis of cerebrovascular disease, any primary neurodegenerative disorder, or any other causes of neuropsychologic disturbances A current diagnosis of active, uncontrolled seizure disorder or major depression, or any other diagnosis that may interfere with the patient's response to study medication An advanced, severe or unstable disease of any type that may interfere with efficacy evaluations Female patients with child-bearing potential who are breast-feeding, pregnant or not practicing non-hormonal contraception Other protocol-defined inclusion/exclusion criteria may apply.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    20 week's treatment with rivastigmine on selective attention compared with placebo in patients with TBI and cognitive impairment

    Secondary Outcome Measures

    Safety of rivastigmine
    Change from baseline to week 20 in cognitive functioning including selective attention, memory, executive function, and global clinical rating

    Full Information

    First Posted
    September 13, 2005
    Last Updated
    November 22, 2011
    Sponsor
    Novartis
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00171795
    Brief Title
    Efficacy and Safety of Rivastigmine in Patients With Traumatic Brain Injury and Cognitive Impairment
    Official Title
    Efficacy and Safety of Rivastigmine in Patients With Traumatic Brain Injury and Cognitive Impairment
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2011
    Overall Recruitment Status
    Completed
    Study Start Date
    November 2002 (undefined)
    Primary Completion Date
    May 2005 (Actual)
    Study Completion Date
    May 2005 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Novartis

    4. Oversight

    5. Study Description

    Brief Summary
    This study is designed to investigate the efficacy and safety of rivastigmine compared with placebo in patients with traumatic brain injury and cognitive impairment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Traumatic Brain Injury
    Keywords
    Traumatic brain injury,, cognitive impairment,, rivastigmine

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    67 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Rivastigmine
    Primary Outcome Measure Information:
    Title
    20 week's treatment with rivastigmine on selective attention compared with placebo in patients with TBI and cognitive impairment
    Secondary Outcome Measure Information:
    Title
    Safety of rivastigmine
    Title
    Change from baseline to week 20 in cognitive functioning including selective attention, memory, executive function, and global clinical rating

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Eligibility Criteria
    Inclusion Criteria: Traumatic brain injury confirmed by available brain imaging (CT or MRI) and be at least 52 weeks post injury Neuropsychologic disturbances indicated by: impaired memory (reduction of below 1 standard deviation (SD) of the mean on the California Verbal Learning Test (CVLT) and impaired executive function (reduction of below 1 standard deviation (SD) of the mean on the Verbal Memory Learning Test (VLMT) and Tower of London Test (ToL) and impaired attention (reduction of below 1 standard deviation (SD) of the mean on the Test Battery for Attentional Performance (TAP) Be required to have had sufficient education to read, write, and effectively communicate Be cooperative, able to ingest oral medication, and able to complete all aspects of the study and capable of doing so, either alone or with the aid of a responsible caregiver according to the investigator's judgement Exclusion Criteria: A current diagnosis of cerebrovascular disease, any primary neurodegenerative disorder, or any other causes of neuropsychologic disturbances A current diagnosis of active, uncontrolled seizure disorder or major depression, or any other diagnosis that may interfere with the patient's response to study medication An advanced, severe or unstable disease of any type that may interfere with efficacy evaluations Female patients with child-bearing potential who are breast-feeding, pregnant or not practicing non-hormonal contraception Other protocol-defined inclusion/exclusion criteria may apply.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Novartis Pharma
    Organizational Affiliation
    Novartis Pharmaceuticals
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Learn more about this trial

    Efficacy and Safety of Rivastigmine in Patients With Traumatic Brain Injury and Cognitive Impairment

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