Phase
Condition
Traumatic Brain Injury
Neurologic Disorders
Memory Loss
Treatment
NE3107
Clinical Study ID
Ages 18-74 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Diagnosis of traumatic brain injury, confirmed by neurologist or other medicalprofessional
Age within range of 18-75 years old
Multidimensional Fatigue Inventory (MFI) score of 27 or greater
Epworth Sleepiness Scale (ESS) score of 10 or greater AND/OR a Pittsburgh Sleep Index (PSI) score of 5 or greater
Ability to Consent: Participants need to be capable of giving informed consent or have a legally authorized representative who can do so.
Ability to participate for the duration of the study
Exclusion
Exclusion Criteria:
- In order for a subject to be considered for this study, he/she may NOT have any ofthe following:
Diagnosis of other chronic Neurological Conditions: Examples are participants with other pre-existing neurological conditions, such as Alzheimer's or Parkinson's Disease or untreated epilepsy.
Severe Psychiatric Illness: Conditions such as schizophrenia, bipolar disorder, or severe depression.
Current diagnosis of Substance Abuse Disorder, including opioid use disorder.
Dysphagia or Significant GI dysmotility or conditions that would significantly impair absorption
Significant language impairment with expressive or receptive aphasia
Hematological or Metabolic derangement or diagnosis of other medical condition that could be negatively affected by participating in this clinical trial.
Pregnant or plans for pregnancy or breastfeeding during the course of the study
Diagnosis of genetic or developmental disorder with cognitive impairment
Use of more than 2 sleep aids including melatonin
Advanced stages of any terminal illness or any active cancer that requires chemotherapy
History of breast cancer
Women with child-bearing potential who are not willing to use a double-barrier birth control method
Males not willing to use a double-barrier birth control method with female sex partners with child-bearing potential
Individuals with hepatic impairment as defined by:
Alanine aminotransferase (ALT) lab values >3x the upper normal limit (UNL)
Aspartate aminotransferase (AST) lab values >3x UNL
OR
History of clinically significant liver disease in the Principal Investigator's medical judgment
Individuals with renal impairment as defined by Creatinine clearance (Cockcroft-Gault formula) of <45 mL/min.
Study Design
Study Description
Connect with a study center
The Regenesis Project
Santa Monica, California 90403
United StatesActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.