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Phase 4 N=31 Other

The Relationship Among Changes in Brain Network Activation in Adult Outpatients With Major Depressive Disorder

Major Depressive Disorder

Enrolled (actual)
31
Serious AEs
0.0%
Results posted
Oct 2021
Primary outcome: Primary: Change in Montgomery and Asberg Depression Rating Scale (MADRS) — 33.28; 16.23 score on a scale — p=<0.001

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
vortioxetine (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Rush University Medical Center
Primary completion
Jan 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Montgomery and Asberg Depression Rating Scale (MADRS)
33.28; 16.23 <0.001 sig
PRIMARY
Change From Baseline to Endpoint in Digital Symbol Substitution Test.
48.24; 55.55 0.012 sig
PRIMARY
BNA Scores Amplitudes
4.04; 3.96; 9.43; 7.13; 6.48; 6.75 0.610
PRIMARY
BNA Scores Latencies
177.37; 177.90; 308.47; 281.38; 370.07; 367.27 0.143
SECONDARY
Changes in Hamilton Depression Rating Scale (HDRS) 17 From Baseline to 8 Week Endpoint
23.76; 11.59 <0.001 sig
SECONDARY
Changes in Hamilton Depression Rating Scale (HDRS) 28 From Baseline to 8 Week Endpoint
28.44; 14.77 <0.001 sig
SECONDARY
Changes in Quick Inventory of Depressive Symptomatology - Self-Report (QIDS-16-SR) From Baseline to 8 Week Endpoint
16.24; 7.91 <0.001 sig
SECONDARY
Changes in Clinical Global Impression Scale (CGI-S) From Baseline to 8 Week Endpoint
4.88; 2.64 <0.001 sig
SECONDARY
Correlations Between BNA Amplitude Scores and Clinical, Cognitive, and Functionality Assessments Using Baseline Scores
4.04; 3.96; 9.43; 7.13; 6.48; 6.75 0.859
SECONDARY
Correlations Between BNA Latency Scores and Clinical, Cognitive, and Functionality Assessments Using Baseline Scores
177.37; 177.90; 308.47; 281.38; 370.07; 367.27 0.881

Summary

The purpose of this study is to explore patterns of Brain Network Activation (BNA) changes from baseline to endpoint on 1) efficacy of core symptoms of Major Depressive Disorder (MDD) and 2) improvement of cognitive dysfunction with acute treatment with flexible dose vortioxetine in adult outpatients with MDD and subjective complaints of cognitive dysfunction.

Eligibility Criteria

Inclusion Criteria

  • The subject has single episode or recurrent MDD (acute onset of recurrence of recurrent MDD with poor inter-episode recovery) (inter-episode periods cannot meet full MDD criteria) as the primary diagnosis according to DSM-IV-TR criteria. The current major depressive episode (MDE) will be confirmed using the Mini International Neuropsychiatric Interview (MINI V6.0.0).
  • The subject has a MADRS total score ≥26.
  • Subject reports subjective cognitive dysfunction (such as difficulty concentrating, slow thinking, and difficulty in learning new things or remembering things).
  • The reported duration of the current MDE is at least 3 months and no longer than 24 months.
  • The subject is a man or woman between 18 and 65 years old, inclusive.
  • Right-handed, normal (corrected) vision, and normal hearing.

Exclusion Criteria

  • The subject has a score of ≥70 on the Digit Symbol Substitution Test (DSST) at the Baseline Visit.
  • Failure to respond to or inability to tolerate an adequate trial of vortioxetine in the past.
  • Exposure to an investigational compound 30 days prior to enrollment
  • Exposure to any psychoactive or otherwise excluded medication within five half-lives of the baseline visit or during the study. Excluded medications include: antidepressants, anxiolytics, anticonvulsants, barbiturates, chloral hydrate, lithium, antipsychotics, benzodiazepines, hypnotics, monoamine oxidase inhibitors (MAOIs), muscle relaxers, triptans, centrally-acting antihistamines, central alpha-2 agonists, decongestants, psychostimulants, dopamine agonists, opioid pain medications, oral corticosteroids, L-methylfolate, S-adenosyl methionine (SAMe), 5-HTP (hydroxytryptophan), St. John's Wort,
  • The subject has 1 or more of the following:
  • Primary psychiatric disorder other than MDD as defined in the Diagnostic and Statistical Manual of Mental Disorders 4 Text Revision (DSM-IV-TR) (as assessed by the MINI, Version 6.0.0).
  • Current or history of attention deficit hyperactivity disorder (ADHD), pervasive developmental disorder, manic or hypomanic episode, schizophrenia, or any other psychotic disorder, including major depression with psychotic features, mental retardation, organic mental disorders, or mental disorders due to a general medical condition as defined in the DSM-IV-TR.
  • Current diagnosis of alcohol or other substance abuse or dependence (excluding nicotine or caffeine) as defined in the DSM-IV-TR that has not been in sustained full remission for at least 6 months (for abuse) and 12 months (for dependence) prior to Screening.
  • Positive urine drug screen prior to Baseline.
  • Presence or history of a clinically significant neurological disorder (including epilepsy).
  • Neurodegenerative disorder (Alzheimer Disease, Parkinson Disease, multiple sclerosis, Huntington Disease, etc).
  • Any unstable medical condition as determined by the principal investigator (PI).
  • Any DSM-IV Axis II disorder that might compromise the study as determined by the PI.
  • The subject has any other disorder for which the treatment takes priority over treatment of MDD or is likely to interfere with study treatment or impair treatment compliance.
  • The subject has physical, cognitive, or language impairment of such severity as to adversely affect the validity of the data derived from the neuropsychological tests.
  • The subject has a significant risk of suicide according to the PI's clinical judgment.
  • The subject, in the opinion of the PI, poses a risk of harm to others.
  • The subject has initiated formal cognitive or behavioral therapy, systemic psychotherapy within less than 6 months of study screening, or has plans to initiate such therapy during the study.
  • The subject has received electroconvulsive therapy, vagus nerve stimulation, or repetitive transcranial magnetic stimulation within 12 months prior to Screening.
  • The current MDE is considered by the PI to have been resistant to 2 adequate antidepressant treatments of at least 6 weeks
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02749721). 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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