search
Back to results

Amantadine for Treatment of Symptoms of the Post-traumatic Confusional State

Primary Purpose

Traumatic Brain Injury, Posttraumatic Confusional State, Delirium

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Amantadine hydrochloride
Placebo capsule
Sponsored by
Methodist Rehabilitation Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury focused on measuring Traumatic Brain Injury, Posttraumatic Confusional State, Delirium, Amantadine, Clinical trial

Eligibility Criteria

16 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Acute Traumatic Brain Injury (≤90 days postinjury)
  • Responsive (not fulfilling criteria for Minimally Conscious State)
  • Meet PTCS criteria on 2 consecutive examinations (as determined by the Confusion Assessment Protocol)
  • Initial neurorehabilitation hospital admission
  • Anticipated ≥2 week length-of-stay after meeting PTCS criteria

Exclusion Criteria:

  • Preexisting seizure disorder
  • Prior history of hospitalization for psychiatric condition

Sites / Locations

  • Methodist Rehabilitation Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Amantadine

Arm Description

Identical capsule to amantadine hydrochloride active intervention, administered twice daily x 14 days

Amantadine hydrochloride 100mg capsule administered twice daily x 14 days

Outcomes

Primary Outcome Measures

Confusion Assessment Protocol (number of symptoms)

Secondary Outcome Measures

number of participants withdrawn from study due to fulfillment of "escape criteria"
Time to reach "non-confused" Confusion Assessment Protocol score

Full Information

First Posted
June 4, 2008
Last Updated
October 17, 2023
Sponsor
Methodist Rehabilitation Center
Collaborators
U.S. Department of Education
search

1. Study Identification

Unique Protocol Identification Number
NCT00693121
Brief Title
Amantadine for Treatment of Symptoms of the Post-traumatic Confusional State
Official Title
Amantadine Hydrochloride for Treatment of Symptoms of the Post-traumatic Confusional State Among Neurorehabilitation Admissions With TBI: A Randomized, Double-Blind, Placebo-Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
April 2003 (undefined)
Primary Completion Date
November 2007 (Actual)
Study Completion Date
March 2019 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Methodist Rehabilitation Center
Collaborators
U.S. Department of Education

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with traumatic brain injury often experience a period of acute confusion that may include agitation as they recover from their injuries. While this confusion generally resolves with time, patients may pose increased risk of injury to themselves or others during this period. Their behavior may also increase stress for family members and interfere with their ability to benefit from rehabilitation therapies. A number of different medications have been used to treat confusion to decrease agitation, decrease risk of injury, and improve participation in rehabilitation therapies. To this point, there has not been a research or scientific basis for knowing which medication is the best for a specific patient. The overall goal of this study is to conduct a scientific investigation to help determine which medication works best to treat confusion. Study hypothesis: Amantadine will reduce the severity and number of symptoms of acute confusion after traumatic brain injury.
Detailed Description
Patients with TBI who require inpatient rehabilitation are frequently confused at the time of admission for rehabilitation. Our investigations of confusion conducted as part of the TBIMSM have clarified the nature of confusion in early recovery after TBI. Early confusion (PTCS) has been found to be a complex syndrome characterized by disorientation, cognitive impairment, restlessness, decreased level of daytime arousal, sleep disturbance, fluctuation of symptoms, and psychotic-type symptoms. PTCS complicates early management of patients with TBI, and may contribute to increased risk of injury to patients and hospital staff, increased stress among family members and staff, decreased participation in therapies, increased cost of care, and an increased likelihood of being discharged to psychiatric or long-term care settings. These facts indicate the need for effective management of PTCS. Consensus regarding optimal treatment of the cognitive and behavioral symptoms encountered among patients with PTCS does not exist currently. While many agents have been tried to address such symptoms in TBI, few have been investigated systematically. These circumstances indicate the need for appropriate clinical trials to provide guidance to clinicians for medical treatment of PTCS. In response, the NIDRR-Traumatic Brain Injury Model System of Mississippi proposed a randomized, double-blinded, placebo-controlled, parallel group trial for the pharmacological treatment of PTCS. The agent selected for this clinical trial is amantadine, an NMDA and indirect dopamine agonist. This agent will be compared to placebo on response measures of efficacy and safety. Study hypothesis: Amantadine will reduce the severity and number of symptoms of PTCS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury, Posttraumatic Confusional State, Delirium
Keywords
Traumatic Brain Injury, Posttraumatic Confusional State, Delirium, Amantadine, Clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
79 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Identical capsule to amantadine hydrochloride active intervention, administered twice daily x 14 days
Arm Title
Amantadine
Arm Type
Active Comparator
Arm Description
Amantadine hydrochloride 100mg capsule administered twice daily x 14 days
Intervention Type
Drug
Intervention Name(s)
Amantadine hydrochloride
Intervention Description
100mg administered orally twice daily x 14 days
Intervention Type
Drug
Intervention Name(s)
Placebo capsule
Intervention Description
capsule, identical to amantadine hydrochloride capsule, administered twice daily x 14 days
Primary Outcome Measure Information:
Title
Confusion Assessment Protocol (number of symptoms)
Time Frame
14 days
Secondary Outcome Measure Information:
Title
number of participants withdrawn from study due to fulfillment of "escape criteria"
Time Frame
14 days
Title
Time to reach "non-confused" Confusion Assessment Protocol score
Time Frame
<14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute Traumatic Brain Injury (≤90 days postinjury) Responsive (not fulfilling criteria for Minimally Conscious State) Meet PTCS criteria on 2 consecutive examinations (as determined by the Confusion Assessment Protocol) Initial neurorehabilitation hospital admission Anticipated ≥2 week length-of-stay after meeting PTCS criteria Exclusion Criteria: Preexisting seizure disorder Prior history of hospitalization for psychiatric condition
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stuart A Yablon, M.D.
Organizational Affiliation
Brain Injury Program, Methodist Rehabilitation Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mark Sherer, Ph.D.
Organizational Affiliation
Department of Research, Memorial Hermann/TIRR, Houston, TX
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Risa N Richardson, Ph.D.
Organizational Affiliation
Polytrauma Program, James A. Haley Veterans Hospital, Tampa, FL
Official's Role
Study Director
Facility Information:
Facility Name
Methodist Rehabilitation Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18164329
Citation
Sherer M, Yablon SA, Nakase-Richardson R, Nick TG. Effect of severity of post-traumatic confusion and its constituent symptoms on outcome after traumatic brain injury. Arch Phys Med Rehabil. 2008 Jan;89(1):42-7. doi: 10.1016/j.apmr.2007.08.128.
Results Reference
background
PubMed Identifier
17178822
Citation
Nakase-Richardson R, Yablon SA, Sherer M. Prospective comparison of acute confusion severity with duration of post-traumatic amnesia in predicting employment outcome after traumatic brain injury. J Neurol Neurosurg Psychiatry. 2007 Aug;78(8):872-6. doi: 10.1136/jnnp.2006.104190. Epub 2006 Dec 18.
Results Reference
background
PubMed Identifier
15895334
Citation
Sherer M, Nakase-Thompson R, Yablon SA, Gontkovsky ST. Multidimensional assessment of acute confusion after traumatic brain injury. Arch Phys Med Rehabil. 2005 May;86(5):896-904. doi: 10.1016/j.apmr.2004.09.029.
Results Reference
background
PubMed Identifier
14660226
Citation
Nakase-Thompson R, Sherer M, Yablon SA, Nick TG, Trzepacz PT. Acute confusion following traumatic brain injury. Brain Inj. 2004 Feb;18(2):131-42. doi: 10.1080/0269905031000149542.
Results Reference
background

Learn more about this trial

Amantadine for Treatment of Symptoms of the Post-traumatic Confusional State

We'll reach out to this number within 24 hrs