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Phase 2 N=247 Basic Science

miRNAs, Suicide, and Ketamine - Plasma Exosomal microRNAs as Novel Biomarkers for Suicidality and Treatment Outcome

Major Depressive Disorder

Enrolled (actual)
247
Serious AEs
2.8%
Results posted
Jul 2022
Primary outcome: Primary: Beck Scale for Suicide Ideation (BSS) — 9.09; 8.46; 1.9 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
ketamine (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Alabama at Birmingham
Primary completion
Dec 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Beck Scale for Suicide Ideation (BSS)
9.09; 8.46; 1.9
SECONDARY
Montgomery Asberg Depression Rating Scale (MADRS)
11.7; 11.56; 8.14
SECONDARY
Beck Depression Inventory (BDI)
18.02; 15.85; 12.12
SECONDARY
Beck Anxiety Inventory (BAI)
6.76; 6.59; 3.31
SECONDARY
Beck Hopelessness Scale (BHS)
8.25; 8.35; 7.22
SECONDARY
4-item Brief Psychiatric Rating Scale (BPRS)
0.02; 0.04; 0.03
SECONDARY
Clinician-Administered Dissociative States Scale (CADSS)
0.5; 0.37; 0.34
SECONDARY
Young Mania Rating Scale (YMRS)
1.61; 2.02; 0.85
SECONDARY
Systematic Assessment for Treatment Emergent Events (SAFTEE)
20.66; 18.67; 11.81

Summary

The purpose of this study is to examine whether neural-derived exosomal miRNAs are differentially expressed that are specific to suicidal ideation or behavior, and which by affecting specific miRNA targets and pathways, are associated with suicidal behavior and response to ketamine. The following groups of subjects will be examined: 1) major depressive disorder (MDD) with a recent suicide attempt (in past 2 weeks), 2) MDD with serious ideation (in the past 7 days) without recent suicide attempt (in the past 6 months), 3) MDD without clinically significant suicidal ideation (in the past 7 days) or recent suicide attempt (in the past 6 months), and 4) healthy controls. Both suicidal and non-suicidal MDD will be given ketamine (0.5 mg/kg, IV) and blood will be drawn at predose, 30 min, 180 min, 24 hours, and 14 days post-infusion to measure changes in miRNAs. As of May 2022, study is in data analysis. Final outcomes will be known once analysis is complete. As of July 2022, all data collection is complete. The primary and secondary data outcome measure results are complete. The investigators are working on final analysis of the mRNA samples, to provide final responses to questions posed in the Detailed Description section below and listed here: 1) whether suicidal ideation or behavior is associated with differences in the expression of specific miRNAs, 2) whether anti-suicidal/antidepressant effects of ketamine is associated with miRNAs changes, and 3) whether miRNA/mRNA-regulatory pathways contribute to suicide pathogenesis and treatment response.

Eligibility Criteria

Inclusion Criteria

  • Age 18-65
  • Physically healthy and capable of undergoing ketamine infusion
  • Willing and able to provide informed consent
  • Diagnosis of Major Depressive Episode (MDE) as determined by the Mini International Neuropsychiatric Interview (MINI) (MDD participants)
  • Hamilton Depression Rating Scale (HAM-D) 21 score ≥ 16 (MDD participants)
  • Suicide attempt occurred within past 2 weeks (MDD Participants with Suicide Attempt)
  • For the time frame of the past 7 days, Columbia-Suicide Severity Rating Scale (C-SSRS) score ≥ 3 (MDD Participants without Suicide Attempt, with Suicidal Ideation)
  • For the time frame of the past 7 days, C-SSRS score 150 and/or diastolic blood pressure >90 at screening
  • A Corrected QT Interval (QTc) > 480 msec as determined by an ECG
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02418195). 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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