Effectiveness of Amantadine Hydrochloride for Treatment of Severe Traumatic Brain Injury (TBI)

Phase 2

Completed

• Conditions: Traumatic Brain Injury
• Interventions: Drug: Amantadine Hydrochloride; Drug: Placebo

• Registration Number: NCT00970944
• Lead Sponsor: JFK Medical Center

Brief Summary

This is a controlled trial of amantadine to improve level of function following severe traumatic brain injury.

The purpose of this study is:

1. To determine whether amantadine hydrochloride, given in a dose of 200-400 mg, improves functional recovery from the vegetative and minimally conscious states

2. To determine whether amantadine-related gains in function persist following drug discontinuation

3. To determine the safety profile of amantadine in patients with disorders of consciousness

Detailed Description

Severe traumatic brain injury may result in severe disorders of consciousness (DOC), including coma, the vegetative state (VS) and the minimally conscious state (MCS). The longer the duration of impaired consciousness, the worse the ultimate functional prognosis, with only about half of those individuals who remain unconscious for a month post-TBI regaining consciousness within a year. The severe functional disability associated with prolonged DOC places enormous emotional, financial, ethical, and logistical strains on caregivers and major resource demands on society. Numerous treatments have been recommended to hasten the return of consciousness or improve the ultimate level of recovery, including various psychotropic drugs, "coma stimulation" therapy and others. However, none of these treatments has proven efficacy in well-controlled research. The main obstacles to Class I evidence in this area have been the small samples of individuals with serious DOC in individual facilities, the variability of recovery trajectories within this heterogeneous population, and the reluctance to undertake placebo controlled trials.

In the proposed study, 7 facilities (including two with TBI Model Systems designations) that participated in a multi-center research network called the Consciousness Consortium, join with four additional brain injury rehabilitation centers (two in the U.S. and two in Europe) and a Data Coordinating Center at Columbia University, to conduct a prospective double blind randomized controlled trial of amantadine hydrochloride. 184 patients who remain in VS or MCS 4 - 16 weeks post-TBI will be randomized in a stratified fashion to 4 weeks of amantadine (200 - 400 mg/day) vs. placebo, followed by a 2-week washout period. The Disability Rating Scale (DRS) will be the primary dependent variable with the Coma Recovery Scale-Revised (CRS-R) serving as a supplementary measure. We hypothesize superior recovery in the amantadine group and maintenance of that advantage after washout. We will also explore whether treatment response differs by time post-injury and by diagnosis (i.e., VS or MCS) at treatment onset, and whether specific outcomes of importance to caregivers are achieved more often in the amantadine group. We have developed plans for intensive education of caregivers and clinicians about this study to address perceived barriers to enrollment and will also use the information gathered during these interactions to develop consumer-oriented dissemination activities. Project outputs and findings will be disseminated to appropriate consumer and professional audiences using a variety of formats and will include: (1) improved family member understanding of DOC which will facilitate improved adjustment and caregiving and (2) clear guidance to clinicians regarding the effectiveness of amantadine for persons with DOC.

Study Timeline

• Study Start: 2003-02
• Study First Submitted: 2009-09-02
• Study First Submitted QC: 2009-09-02
• Study First Posted: 2009-09-03
• Primary Completion: 2010-03
• Study Completion: 2010-03
• Results First Submitted: 2011-12-12
• Status Verified: 2012-09
• Results First Submitted QC: 2012-09-11
• Last Update Submitted: 2012-09-11
• Results First Posted: 2012-09-24
• Last Update Posted: 2012-09-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 184

Inclusion Criteria

• Individuals between ages 16 and 65 with traumatic brain injury as defined by the TBI Model System syllabus (i.e., damage to brain tissue caused by an external mechanical force as evidenced by loss of consciousness or post-traumatic amnesia due to brain trauma, skull fracture, or objective neurological findings that can be reasonably attributed to TBI on physical or mental status examination).
• Individuals are at least 4 weeks but less than 16 weeks post-injury and have a Disability Rating Scale (DRS) score at enrollment of 12 or greater, and no consistent command following or functional communication (as defined by the JFK.

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Exclusion Criteria

• Women who are pregnant,
• Individuals with missile-type penetrating brain injury,
• Premorbid major CNS/developmental abnormality (e.g., mental retardation, prior significant brain damage, etc.),
• History of more than 1 seizure (clinical or electrographic, but not including epileptiform or other irritative discharges) in the 4 weeks prior to enrollment (individuals with premorbid idiopathic epilepsy are eligible to enroll under two conditions: a) if their pre-injury seizure frequency was less than once/month and they have had no more than 1 seizure/month since injury and b) if a clear provocation was present that would otherwise disqualify a subject, the subject can be enrolled, since these events would not be considered idiopathic),
• Prior exposure to AH post-TBI,
• Unwillingness to discontinue or change confounding psychotropic drugs prior to enrollment, OR
• Allergy or medical contraindication to AH and significant impairment of renal function (as evidenced by a calculated creatinine clearance of < 60 ml/min).

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Amantadine HCL	Amantadine Hydrochloride	100mg BID administered for 2 weeks, then increased to 150mg BID in week 3 if change on primary outcome measure (ie Disability Rating Scale, DRS) was less than 2 points after week 2. If change in DRS score remained less than 2 points after week 3, dose was increased to 200mg BID in week 4.
Placebo	Placebo	-

Primary Outcome Measures

Name	Time	Method
Disability Rating Scale: Functional Status	Randomization and weekly for 6 weeks. The primary study endpoint was week 4 and drug washout was week 6.	Measure of function after traumatic brain injury (TBI) intended to measure function from "coma to community." Minimum score= 0; Maximum score= 29 (High scores are indicative of greater degree of disability).

Secondary Outcome Measures

Name	Time	Method
JFK Coma Recovery Scale-Revised: Neurobehavioral Status	Week 4 (primary endpoint); Week 6 (post-washout)	Measure of neurobehavioral function and clinical change for individuals with severe alterations of consciousness.; Minimum score= 0; Maximum score= 23 (Higher scores are indicative of a higher-level of neurobehavioral function).

Trial Locations

Locations (11)

Methodist Rehabilitation Center; 🇺🇸 Jackson, Mississippi, United States

Braintree Rehabilitation Hospital; 🇺🇸 Braintree, Massachusetts, United States

Columbia University; 🇺🇸 New York, New York, United States

Bryn Mawr Rehabilitation Hospital; 🇺🇸 Malvern, Pennsylvania, United States

Hvidovre University Hospital; 🇩🇰 Hvidovre, Denmark

Neurologische Klinik Bad Aibling; 🇩🇪 Bad Aibling, Germany

Moss Rehabilitation Research Institute; 🇺🇸 Elkins Park, Pennsylvania, United States

Sunnyview Rehabilitation Hospital; 🇺🇸 Schenectady, New York, United States

Charlotte Rehabilitation Center; 🇺🇸 Charlotte, North Carolina, United States

Texas NeuroRehabilitation Center; 🇺🇸 Austin, Texas, United States

Fachkrankenhaus Neresheim; 🇩🇪 Neresheim, Germany