Phase 2
N=247
miRNAs, Suicide, and Ketamine - Plasma Exosomal microRNAs as Novel Biomarkers for Suicidality and Treatment Outcome
Major Depressive Disorder
Bottom Line
View on ClinicalTrials.gov: NCT02418195 ↗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
| Outcome | Result | p-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
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.