Status:
UNKNOWN
Antidepressant Discontinuation in Treatment Resistant Depression
Lead Sponsor:
University of Louisville
Conditions:
Treatment Resistant Depression
Eligibility:
All Genders
18-70 years
Phase:
NA
Brief Summary
The purpose of this study is to compare the effects on depressive symptoms of subjects who discontinue serotonergic antidepressants (a certain type of antidepressant, such as Prozac, that works on ser...
Eligibility Criteria
Inclusion
- Subjects must be a man or woman 18 to 70 years of age, inclusive.
- Subject must meet criteria for a major depressive disorder as confirmed by the Mini International Neuropsychiatric Interview \[MINI\].
- Subjects must have a current Treatment-Resistant Depression as defined below.
- Subjects must have been taking serotonergic antidepressants (serotonin reuptake inhibitor or monoamine oxidase inhibitor) for at least 2 years but not more than 4 years, and have failed 2 previous medication trial for the current episode. Current Montgomery-Åsberg Depression Rating Scale \[MADRS\] score must be equal to or more than 25.
- Subject must be medically stable.
- Female subjects must have a negative urine pregnancy test at screening, and agree to avoid pregnancy during the study.
- Each subject must sign an informed consent form indicating that he/she understands the purpose of the study and the procedures required and are willing to participate in the study.
- Subject must be able to participate in symptom measurement.
Exclusion
- Subject has a current Diagnostic and Statistical Manual of Mental Disorders-5 \[DSM-5\] diagnosis of bipolar disorder or has a positive screening for bipolar disorder by Mini International Neuropsychiatric Interview \[MINI\] or Mood Disorder Questionnaire \[MDQ\].
- Subject has a current DSM-5 diagnosis of schizophrenia, schizoaffective disorder, autistic disorder, or intellectual disability.
- Subject has a substance use disorder (except for nicotine or cannabis) within 3 months prior to screening or has a positive drug screen test for any recreational drugs at the time of screening with the exception of Cannabis.
- Subject has evidence of any clinically significant, unstable medical problems that may create a safety risk for a subject, interfere with study participation, or make results difficult to interpret.
- Subject is at imminent risk of suicide according to the investigator's clinical judgment and/or a Columbia-Suicide Severity Rating Scale (C-SSRS) 3 or more at any time in the study.
- Subject is a woman who is pregnant, breast-feeding or planning to become pregnant while enrolled in the study.
- Subject has any condition (according to the investigator) for which participation will not be the best interest for the subject or it can prevent, limit or confound the protocol-specified assessments.
Key Trial Info
Start Date :
June 20 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2024
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT03786614
Start Date
June 20 2019
End Date
December 1 2024
Last Update
August 18 2023
Active Locations (1)
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1
University of Louisville, Department of Psychiatry and Behavioral Sciences
Louisville, Kentucky, United States, 40202