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N/A N=6 Treatment

Deep Brain Stimulation for the Treatment of Traumatic Brain Injury

TBI (Traumatic Brain Injury)

Enrolled (actual)
6
Serious AEs
33.3%
Results posted
Dec 2022
Primary outcome: Primary: Percent Change in Trail Making Test Part B Time to Completion — -25.6 percent change in time

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Deep brain stimulation (Device)
Age
Adult · 22+ yrs
Sex
All
Sponsor
Jaimie M. Henderson
Primary completion
Oct 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Percent Change in Trail Making Test Part B Time to Completion
-25.6
SECONDARY
Percent Change in Trail Making Test Part A Time to Completion
-27.4
SECONDARY
Percent Change in Traumatic Brain Injury Quality of Life - Executive Function Short Form (TBI-QOL) Scale Score
28.0
SECONDARY
Percent Change Traumatic Brain Injury Quality of Life - Attention/Concentration Short Form Scale Score
66.7
SECONDARY
Percent Change in Traumatic Brain Injury Quality of Life - Fatigue Short Form Scale Score
2.9
SECONDARY
Percent Change in Rivermead Post-Concussion Symptom Questionnaire Scale Score
-36.6
SECONDARY
Percent Change in Ruff 2 and 7 Automatic Detection Speed Score
21.1
SECONDARY
Percent Change in Ruff 2 and 7 Automatic Detection Accuracy Score
5.2
SECONDARY
Percent Change in Ruff 2 and 7 Controlled Search Speed Score
17.3
SECONDARY
Percent Change in Ruff 2 and 7 Controlled Search Accuracy Score
2.7
SECONDARY
Percent Change in Patient Health Questionnaire - 9 Scale Score.
-41.7
SECONDARY
Number of Participants With ≥1 Point Increase in Glasgow Outcome Scale - Extended Scale Score
2

Summary

This study involves the treatment of cognitive impairment secondary to moderate to severe brain injury using central thalamic deep brain stimulation. Although all patients will receive stimulation continuously through a surgically implanted pacemaker-like device, half of the patients will have the device deactivated during a blinded assessment phase. The device will be reactivated following this assessment and patients will have the option to continue stimulation in an open-label continuation.

Eligibility Criteria

Inclusion Criteria

  • History of moderate to severe TBI based on worst GCS score within first 48 hours of injury (acceptable GCS range = 3-12)
  • Age 22-60
  • At least 24 months from date of onset
  • Fluent in English and able to independently provide consent
  • Rating of upper moderate disability to lower good recovery on the Glasgow Outcome Scale-Extended (GOSE) at time of enrollment (acceptable GOSE range 5-7)
  • Failure to return to pre-injury level of vocational or educational function
  • Either receiving no CNS stimulants or other medications known to affect cognitive function, or on stable doses of these medications for the last three months

Exclusion Criteria

  • History of major developmental, neurologic, psychiatric or substance use disorder with evidence of disability prior to onset of TBI
  • Major medical co-morbidities including: end stage renal failure, severe heart failure, coagulopathy, severe respiratory problems, severe liver failure, uncontrolled hypertension or other significant medical co morbidities
  • Have had a documented seizure within 3 months of study screening (subjects may re-screen if seizure free after initial screen failure)
  • Malignancy with < 5 years life expectancy
  • Untreated / uncontrolled (severe at the time of enrollment) depression or other psychiatric disorder
  • Women of childbearing age who do not regularly use an accepted contraceptive method
  • Inability to stop anticoagulation therapy or platelet anti-aggregation therapy before, during and after surgery
  • Previous DBS or other brain implants
  • Previous ablative intracranial surgery
  • Implantable hardware not compatible with MRI
  • Condition requiring diathermy after DBS implantation
  • Hardware, lesions or other factors limiting placement of electrodes in optimal target location in the judgment of the operating surgeon
  • Concurrent enrollment in any other clinical trial
  • Any condition or finding that, in the judgment of the PI, significantly increases risk or significantly reduces the likelihood of benefit from DBS
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02881151). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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