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Use of Risperidone in ECT for Treatment Resistant Depression

Primary Purpose

Major Depression

Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Risperidone
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depression focused on measuring mood disorder, affective disorder, depression, treatment-resistant

Eligibility Criteria

18 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age between 18 to 89 years, inclusive Male or female Inpatient or outpatient ECT with a current diagnosis of unipolar or bipolar depression, with or without psychosis, according to DSM-IV criteria. HAM-D (17-item) score > 17 and MADRS score > 18 at screening and at first treatment session. Exclusion Criteria: MMSE < 23 Inability to consent to ECT Current diagnosis of schizophrenia or schizoaffective disorder Current diagnosis of Parkinson's Disease or any Dementia, including Lewy Body Disease History of allergic reaction to risperidone History of Neuroleptic Malignant Syndrome Current pregnancy or positive urine pregnancy test Women who are breast-feeding Active alcohol or illicit substance abuse

Sites / Locations

  • UCLA Npi&H

Outcomes

Primary Outcome Measures

Scores on depression scales after 6 ECT treatments

Secondary Outcome Measures

Scores on Clinical Global Impression Scales and Symptom Checklist

Full Information

First Posted
September 13, 2005
Last Updated
May 17, 2006
Sponsor
University of California, Los Angeles
Collaborators
Janssen, LP
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1. Study Identification

Unique Protocol Identification Number
NCT00203723
Brief Title
Use of Risperidone in ECT for Treatment Resistant Depression
Official Title
A Comparison Study of Combined ECT and Risperidone Versus ECT Alone for Treatment Resistant Depression.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2006
Overall Recruitment Status
Terminated
Study Start Date
March 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of California, Los Angeles
Collaborators
Janssen, LP

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine if the combination of risperidone and ECT improves a patient's response in depression compared to ECT alone.
Detailed Description
Medication resistance to antidepressant therapy, or Treatment-Resistant Depression (TRD), is the main reason, if not main indication, for which patients are presently referred for electroconvulsive therapy (ECT) in hopes of a rapid, definitive response (APA 2001 ECT Task Force Report). While the causes of TRD remain unclear, this category of patients includes those who have incomplete remission, those who relapse rapidly and frequently, those who have psychotic depression, those who develop chronic depression, and those who often have comorbid medical and psychiatric illness (Sackeim 2001, Sharma 2001, Fava and Davidson 1996, Thase 1995). Moreover, while increased age per se is not a barrier to antidepressant response, many elderly, especially those with comorbid medical or neurological illness, are unable to tolerate courses of aggressive pharmacotherapy or seem to have a less robust response to pharmacotherapy, and possibly to ECT alone, with significant residual functional and cognitive impairment (Reynolds 1998, Stoudemire 1998, Lebowitz 1997, Gurland 1991). Compared to patients who are not medication resistant, who generally retain the highest likelihood of response to ECT alone, patients with TRD have a lower response rate to ECT with average estimates of response to ECT alone between 50-60% (APA 2001 ECT Task Force). Additionally, while ECT for most patients may provide acute remission, those patients with TRD remain at high risk for rapid relapse (Sackeim 2001, Petrides 2001, Sackeim 1990, Aronson 1987). Consequently, ECT alone may be insufficient to achieve remission or to prevent relapse. Interestingly, resistance to some types of medication was found also to predict resistance to ECT alone, i.e., resistance to tricyclic antidepressants correlated with a less likely response to ECT, though the same prediction did not hold for serotonin reuptake inhibitors (Prudic 1996, Prudic 1990). In general, for some patients with TRD, studies support the use of combined medication approaches, and specifically, have demonstrated the safety, tolerability and effectiveness of an antidepressant with an antipsychotic medication, though usually for patients with comorbid psychosis (Wheeler 2000, Shelton 1999, Barak 1999). Case reports exist in the ECT literature about the safety and tolerability of ECT and antipsychotics, and improved efficacy, albeit generally for patients with psychotic depression or other treatment resistant psychoses (Kupchik 2000, Bhatia 1998, Ranjan 1996, Farah, Beale, and Kellner 1995, Minter 1979). However, no studies systematically, or prospectively, investigate whether the specific combination of ECT plus an atypical antipsychotic offers a true treatment alternative to improved efficacy of ECT for patients with TRD. This study reviews the experience and outcome of combining ECT and an atypical antipsychotic medication, risperidone, for TRD in various populations in an academic, university-based setting, and furthermore, explores in a pilot randomized open-label study whether ECT plus risperidone bears closer scrutiny in more rigorous study designs as a novel treatment approach.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depression
Keywords
mood disorder, affective disorder, depression, treatment-resistant

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
45 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Risperidone
Primary Outcome Measure Information:
Title
Scores on depression scales after 6 ECT treatments
Secondary Outcome Measure Information:
Title
Scores on Clinical Global Impression Scales and Symptom Checklist

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 18 to 89 years, inclusive Male or female Inpatient or outpatient ECT with a current diagnosis of unipolar or bipolar depression, with or without psychosis, according to DSM-IV criteria. HAM-D (17-item) score > 17 and MADRS score > 18 at screening and at first treatment session. Exclusion Criteria: MMSE < 23 Inability to consent to ECT Current diagnosis of schizophrenia or schizoaffective disorder Current diagnosis of Parkinson's Disease or any Dementia, including Lewy Body Disease History of allergic reaction to risperidone History of Neuroleptic Malignant Syndrome Current pregnancy or positive urine pregnancy test Women who are breast-feeding Active alcohol or illicit substance abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Randall Espinoza, MD, MPH
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA Npi&H
City
Los Angeles
State/Province
California
ZIP/Postal Code
90024
Country
United States

12. IPD Sharing Statement

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Use of Risperidone in ECT for Treatment Resistant Depression

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