Continuation Electroconvulsive Therapy (C-ECT) for Relapse Prevention in Major Depression

Depression Clinical Trial

Official title:

Continuation Electroconvulsive Therapy Associated With Pharmacotherapy Versus Pharmacotherapy Alone for Relapse Prevention in Major Depression. A Clinical, Controlled, Prospective and Randomized Trial

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01305707
• Other study ID #: TECHUB2007
• Status: Terminated
• Phase: Phase 4
• First received: February 28, 2011
• Last updated: August 28, 2015
• Start date: July 2009
• Est. completion date: July 2014

Study information

• Verified date: August 2015
• Source: Hospital Universitari de Bellvitge
• Contact: n/a
• Is FDA regulated: No
• Health authority: Agency of Medicines and Sanitary Products: SpainEuropean Medicines Agency: Europe
• Study type: Interventional

Clinical Trial Summary

OBJECTIVES:

To evaluate the comparative efficacy and security of Continuation Electroconvulsive Therapy associated with pharmacotherapy versus pharmacotherapy alone in the prevention of depressive relapse.

METHODS:

Demographic and clinical variables will be collected and side effects scales and neurocognitive battery will be performed. Variables of efficacy: relapse percentage in both groups in one year (primary variable); time without relapse. Main variable of security: occurrence of side effects and neurocognitive performance.

DESIGN: Randomized controlled clinical trial.

SAMPLE:

104 outpatients diagnosed with unipolar depression (DSM-IV-R criteria) who had remitted with a course of bilateral ECT. They will be randomized to two groups of treatment.

SETTING: Psychiatry Department at Bellvitge University Hospital.

ANALYSIS: Descriptive analysis of clinical variables; survive analysis and Cox model of regression.

Description:

Major Depressive Disorder (MDD) is a severe psychiatric disorder that affects more than 6 million people in our country and has a life prevalence of 8.9% for men and 16. 5% for women (Haro et al, 2007). Besides, in recent decades, its incidence is increasing (Kessler et al, 2004). MDD has high recurrence rates and 25% of the cases develop chronification. Moreover it can occur at any age leading to severe disability. The majority of studies published in this field demonstrated the efficacy of antidepressant treatment in a short or medium-term basis, but there is a lack of long-term clinical trials regarding antidepressant efficacy and published ones present methodological problems. At present, a line of fundamental research in therapeutics includes pragmatic studies because they can answer crucial and specific questions in clinical practice. Therefore, the aim of this project is to conduct a pragmatic, parallel, randomized trial with 2 treatment arms to answer a key question of great interest to psychiatrists: Is it more effective to extend the use of ECT as maintenance therapy (together with drug therapy) rather than just using drug therapy in patients that previously required an acute ECT course for a depressive episode? This study is a controlled randomized clinical trial that starts after the remission of the acute depressive episode. Once patients have clinically remitted they will be randomized in two groups:

1. C-ECT together with pharmacotherapy (same treatment used in the acute episode).

2. Maintenance pharmacotherapy treatment (same treatment used in the acute episode).

Consolidation treatment with ECT will be considered finished after 9 months of being started, at which time patients will stay only on the pharmacological treatment they already had. The study will be completed within 15 months of patient inclusion (six months after the end of C-ECT). Patient assessment and follow-up will be conducted by participant researchers. Blind rater will conduct clinical and adverse effects ratings. A neuropsychologist will conduct neuropsychological assessments.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 104
• Est. completion date: July 2014
• Est. primary completion date: July 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• MDD diagnosis by DSM IV-TR.

• ECT requirement during acute episode. Therapeutic indication will be based on clinical criteria, following APA guidelines. During the acute episode, patients will be controlled by the usual clinical care team.

• Complete clinical remission (HDRS < or = 7 across two weeks).

• Appropriate intellectual level that allows adequate communication.

• Women of childbearing potential must use contraceptive methods.

• Signed Consent form.

• Other axis I or II diagnosis by DSM-IV-TR, except for nicotine dependence.

• To be in maintenance ECT program.

• To receive ECT during the previous three months of the acute episode.

• Pregnancy or breastfeeding.

Exclusion Criteria:

• Other axis I or II diagnosis by DSM-IV-TR, except for nicotine dependence.

• To be in maintenance ECT program.

• To receive ECT during the previous three months of the acute episode.

• Pregnancy or breastfeeding.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Depression
• Depressive Disorder
• Depressive Disorder, Major

Intervention

Device:
• C-ECT
C-ECT will be administered through a Thrymatron System IV device (Somatics, LLC, ISO 13485:2003). Electrode placement will be bilateral and energy administered during consolidation treatment will be same used in the acute episode. C-ECT will be given weekly for the first month, fortnightly for the following two months and monthly during the next 6 months. A total of 14 C-ECT sessions will be given over 9 months of treatment. Pharmacotherapy will remain unchanged since the acute episode to the end of the study. Drugs will be obtained as usually from the National Health System and will be prescribed according to data sheet and it will have a duration of 15 months.

Drug:
• PHARMACOTHERAPY
Pharmacotherapy will remain unchanged since the acute episode to the end of the study. Psychotropics will be obtained as usually from the National Health System and will be prescribed according to data sheet and will have a 15 month duration.

Locations

Country	Name	City	State
Spain	Hospital Universitari de Bellvitge, IDIBELL	Barcelona
Spain	Hospital Universitari de Bellvitge	Hospitalet de Llobregat	Barcelona
Spain	Corporació Sanitària Parc Tauli	Sabadell	Barcelona

Sponsors (1)

Lead Sponsor	Collaborator
Hospital Universitari de Bellvitge

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Hamilton Depression Rating Scale 21 items (HDRS-21)	HDRS-21 will measure the relapse year in each group. Relapse will be defined as the reappearance of relevant symptoms after resolutin of the acute episode, measured by a scoring in HDRS-21 between 15-17 over two following measures or a HDRS>18 score in a single measure.	One year. HDRS will be assessed in each follow-up visit (weekly the first month, fortnightly the second and third month, monthly the following 6 months and quarterly at 12 and 15 months).	No
Secondary	Mini-Mental State Examination (MMSE 35)	Assessment of general cognitive status.	Basal, at 8 months and 12 months	Yes
Secondary	UKU - Adverse effects rating scales	Qualitiative measure of side effects in each treatment group.	Every assessment (weekly, fortnightly, monthly and quarterly) till the month 15 of the follow-up.	Yes
Secondary	Demographical Data Memory (MEDABI-20)	Descriptive measure of cogntive status.	Basal, at 8 months and 12 months	Yes
Secondary	Rey Figure	Measure of visual perception, concentration and memory.	Basal, at 8 months and 12 months	Yes
Secondary	Trail Making Test A	Measure of attention and cognitive flexibility.	Basal, at 8 months and 12 months	Yes
Secondary	Trail Making Test B	Measure of attention and cognitive flexibility.	Basal, at 8 months and 12 months	Yes
Secondary	Stroop Test	Measure of selective attention, cognitive flexibility and processing speed as well as executive function.	Basal, at 8 months and 12 months	Yes
Secondary	Direct and inverse digits (WAIS, Weschler Adults Intelligence Sacle).	Measure of general intelligence and attention	Basal	No
Secondary	Vocabulary WAIS (Weschler Adults Intelligence Scale)	Measure of general intelligence	Basal	No
Secondary	Frequency Hospitalization Quotient	Measure of number of hospitalization per year.	One year	No
Secondary	Hospital Day Quotient (HDQ)	Number of days hospitalized per year.	One year	No