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The Relationship Between Traumatic Brain Injury and Dopamine (a Chemical in the Brain)

Primary Purpose

Traumatic Brain Injury

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Methylphenidate
Placebo
Sponsored by
Imperial College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury

Eligibility Criteria

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

Inclusion Criteria:

  • a diagnosis of a moderate-severe traumatic brain injury (as defined by the Mayo TBI severity classification system) at least 3 months prior to recruitment into the study
  • age between 20 and 65 years
  • capable of giving written informed consent subjective complaint of cognitive difficulties by the participant, treating clinician, or caregiver

Exclusion Criteria:

  • unwillingness or inability to follow the procedures required
  • significant neurological or psychiatric illness diagnosed prior to the TBI
  • family history of a first degree relative with a psychotic illness
  • currently participating in a clinical trial or has done so within 1 month before screening
  • use of any medication or substance that, in the opinion of the investigators, would interfere with the study or compromise participant safety
  • history of a drug or other allergy that, in the opinion of the investigators, contraindicates their participation in the study
  • history of current or past drug or alcohol addiction
  • female participants who are breast feeding or pregnant (positive pregnancy test) or plan to become pregnant during the study
  • positive urine drug screen
  • contraindication to MRI scanning, assessed by a standard pre-MRI questionnaire
  • contraindication to the use of methylphenidate (including medications deemed to have a potentially serious interaction with methylphenidate as per the British National Formulary)
  • clinical evidence of motor symptoms of Parkinsonism as assessed by a Neurologist

Sites / Locations

  • Imperial College

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Methylphenidate

Sugar pill

Arm Description

2 weeks of 0.3mg/kg twice daily of methylphenidate to the nearest 5mg

2 weeks of twice daily placebo

Outcomes

Primary Outcome Measures

The change in Choice Reaction Time task with methylphenidate treatment in patients and its relationship to specific binding ratio (SBR) of the dopamine transporter (DAT) in the striatum.

Secondary Outcome Measures

Full Information

First Posted
November 25, 2013
Last Updated
January 9, 2017
Sponsor
Imperial College London
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1. Study Identification

Unique Protocol Identification Number
NCT02015949
Brief Title
The Relationship Between Traumatic Brain Injury and Dopamine (a Chemical in the Brain)
Official Title
The Control of Brain Networks After Traumatic Brain Injury: a Neuroimaging and Neuropsychological Study of Dopamine and Cognition
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Traumatic brain injury (TBI) is the most common cause of death and disability in young adults. Patients can experience significant problems with concentration, attention, and memory (so called 'cognitive impairments') following TBI. These cognitive impairments can drastically impact on a patient's well-being, and can lead to significant economic and social consequences. Roughly a quarter of TBI patients improve but an equal number deteriorate over time. The investigators know little about why patients vary so much in how they recover. Crucially, the investigators have no treatments to improve brain functioning or recovery after TBI. Trials investigating ways of protecting the brain just after injury have been disappointing. An alternative strategy, however, is to improve the function of brain regions that remain intact, but that function inefficiently after TBI. The investigators know that dopamine (a chemical in the brain) is known to influence many brain functions and the investigators know that pathways in the brain that use dopamine are affected by TBI. In humans, drugs that increase dopamine in the brain, such as methylphenidate, are sometimes used to enhance cognitive function after TBI, but the response to treatment can be highly variable between patients. Therefore, what is needed in the clinic is a way to target the use of these drugs to patients who are likely to respond. In a single centre study, the investigators will use SPECT (Single Photon Emission Tomography) imaging to measure dopamine levels in the brain. MRI (Magnetic Resonance Imaging) scans will assess brain structure and function. The investigators will test whether treatment with methylphenidate improves cognitive functions in TBI patients who have ongoing cognitive problems, whether the mechanism involves a normalisation of brain functioning and whether brain dopamine levels can predict the magnitude of any improvement in symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Methylphenidate
Arm Type
Active Comparator
Arm Description
2 weeks of 0.3mg/kg twice daily of methylphenidate to the nearest 5mg
Arm Title
Sugar pill
Arm Type
Placebo Comparator
Arm Description
2 weeks of twice daily placebo
Intervention Type
Drug
Intervention Name(s)
Methylphenidate
Intervention Description
Cross-over design comparing methylphenidate 0.3 mg/kg (to nearest 5mg) twice daily to placebo
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Twice daily placebo tablet for two weeks
Primary Outcome Measure Information:
Title
The change in Choice Reaction Time task with methylphenidate treatment in patients and its relationship to specific binding ratio (SBR) of the dopamine transporter (DAT) in the striatum.
Time Frame
On completion of the four week drug trial phase

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: a diagnosis of a moderate-severe traumatic brain injury (as defined by the Mayo TBI severity classification system) at least 3 months prior to recruitment into the study age between 20 and 65 years capable of giving written informed consent subjective complaint of cognitive difficulties by the participant, treating clinician, or caregiver Exclusion Criteria: unwillingness or inability to follow the procedures required significant neurological or psychiatric illness diagnosed prior to the TBI family history of a first degree relative with a psychotic illness currently participating in a clinical trial or has done so within 1 month before screening use of any medication or substance that, in the opinion of the investigators, would interfere with the study or compromise participant safety history of a drug or other allergy that, in the opinion of the investigators, contraindicates their participation in the study history of current or past drug or alcohol addiction female participants who are breast feeding or pregnant (positive pregnancy test) or plan to become pregnant during the study positive urine drug screen contraindication to MRI scanning, assessed by a standard pre-MRI questionnaire contraindication to the use of methylphenidate (including medications deemed to have a potentially serious interaction with methylphenidate as per the British National Formulary) clinical evidence of motor symptoms of Parkinsonism as assessed by a Neurologist
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David J Sharp
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Imperial College
City
London
Country
United Kingdom

12. IPD Sharing Statement

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The Relationship Between Traumatic Brain Injury and Dopamine (a Chemical in the Brain)

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