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Amantadine for Treatment of Symptoms of the Post-Traumatic Confusional State
This study is ongoing, but not recruiting participants.
Study NCT00693121   Information provided by Methodist Rehabilitation Center
First Received: June 4, 2008   Last Updated: June 5, 2008   History of Changes

June 4, 2008
June 5, 2008
April 2003
November 2007   (final data collection date for primary outcome measure)
Confusion Assessment Protocol (number of symptoms) [ Time Frame: 14 days ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00693121 on ClinicalTrials.gov Archive Site
  • number of participants withdrawn from study due to fulfillment of "escape criteria" [ Time Frame: 14 days ] [ Designated as safety issue: Yes ]
  • Time to reach "non-confused" Confusion Assessment Protocol score [ Time Frame: <14 days ] [ Designated as safety issue: No ]
Same as current
 
Amantadine for Treatment of Symptoms of the Post-Traumatic Confusional State
Amantadine Hydrochloride for Treatment of Symptoms of the Post-Traumatic Confusional State Among Neurorehabilitation Admissions With TBI: A Randomized, Double-Blind, Placebo-Controlled Trial

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.

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.

Phase IV
Interventional
Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
  • Traumatic Brain Injury
  • Posttraumatic Confusional State
  • Delirium
  • Drug: Amantadine hydrochloride
  • Drug: Placebo capsule
  • Placebo Comparator: Identical capsule to amantadine hydrochloride active intervention, administered twice daily x 14 days
  • Active Comparator: Amantadine hydrochloride 100mg capsule administered twice daily x 14 days

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
79
June 2008
November 2007   (final data collection date for primary outcome measure)

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
Both
 
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00693121
Theresa San Augustin, National Institute for Disability and Rehabilitation Research
MethodistRC Project 1, NIDRR grant #: H133A020514
Methodist Rehabilitation Center
Department of Education
Principal Investigator: Stuart A Yablon, M.D. Brain Injury Program, Methodist Rehabilitation Center
Study Director: Mark Sherer, Ph.D. Department of Research, Memorial Hermann/TIRR, Houston, TX
Study Director: Risa N Richardson, Ph.D. Polytrauma Program, James A. Haley Veterans Hospital, Tampa, FL
Methodist Rehabilitation Center
June 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP