Phase 4
Completed N=54
Paliperidone and Lithium in the Treatment of Suicidality - Treatment Indication and Epigenetic Regulation
Source: ClinicalTrials.gov NCT01134731 ↗Enrolled (actual)
54
Serious AEs
0.0%
Results posted
Jan 2016
Primary outcomePrimary: Mean Score of Beck Scale for Suicidal Ideation of Three Treatment Groups (Paliperidone, Lithium and Placebo) After 3 Months of Treatment — 22.1; 22.1; 21.3 units on a scale
Summary
The study aims to use a combined clinical and translational approach to identify an efficient pharmacotherapy for the acute management of suicidality and the epigenetic regulation associated with the treatment.The primary objective is a clinical trial to compare the efficacy of paliperidone versus lithium and placebo as adjunctive therapy to the standard of care antidepressants in the acute management of suicidality in depressed subjects.
Specific Aims 1 and 2 are described in detail below. Analysis for Specific Aim 2 is still underway.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean Score of Beck Scale for Suicidal Ideation of Three Treatment Groups (Paliperidone, Lithium and Placebo) After 3 Months of Treatment |
22.1; 22.1; 21.3 | — |
| SECONDARY Mean Score of Montgomery-Asberg Depression Scale of Three Treatment Groups (Paliperidone, Lithium and Placebo) After 3 Months of Treatment |
37.5; 39.6; 39.2 | — |
Eligibility Criteria
Inclusion Criteria
- Male and female subjects who are able to provide informed consent
- 19-65 years of age
- Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) diagnosis of MDD by MINI International Neuropsychiatric Interview (MINI) and confirmed by psychiatric interview
- Currently experiencing a depressive episode with suicidality (defined as having current suicidal thoughts occurring at least 3 out of 7 days in a week).
- Montgomery-Asberg Depression Rating Scale (MADRS) must include a total score > 25 and a suicidal sub-score > 4.
Exclusion Criteria
- Depressed patients without suicidality, patients with severe psychotic features or with primary diagnoses of bipolar disorder (BD), schizophrenia, schizoaffective disorder, or generalized anxiety disorder (GAD), and subjects who have been taking lithium or an antipsychotic in the past 2 weeks
- Those with uncontrolled medical illnesses. Participants must be on any new medications for at least 30 days to be considered medically stable.
- For patients with panic disorder, post-traumatic stress disorder (PTSD), borderline personality disorder (BPD), etc. be sure that MDD is the primary diagnosis. When in doubt, decisions will be made on a case-by-case basis.
- Pregnant women.
- Allergic to paliperidone, to any other ingredient in paliperidone ER or paliperidone palmitate, or to risperidone.
Data sourced from ClinicalTrials.gov (NCT01134731). 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. Informational only — not medical advice.