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Effects of Electroconvulsive Therapy (ECT) on Serotonin-1A Receptor Binding

Primary Purpose

Unipolar Depression

Status
Completed
Phase
Phase 4
Locations
Austria
Study Type
Interventional
Intervention
ECT
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Unipolar Depression

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female
  • Age 18 - 65 years
  • ICD-10 diagnosis of severe unipolar depression (ICD-10: F32.2, F32.3; F33.2, F33.3)
  • A score of 23 or greater on the 17-item HAM-D
  • Signed informed consent form
  • Negative urine pregnancy test in women at the screening visit and at PET days
  • Antidepressive and antipsychotic medication in a steady state for at least 10 days prior to inclusion
  • Anesthesiological approval for ECT

Exclusion Criteria:

  • Concomitant major internistic or neurological illness
  • Clinically relevant abnormalities on a general physical examination and routine laboratory screening
  • Current substance abuse, addiction
  • Current or past history of schizophrenia or schizoaffective disorder
  • Exposure to artificial radiation as volunteer in clinical studies within 10 years prior to inclusion into the present study
  • Previous treatments with electroconvulsive therapy
  • Treatment (< 1 months before screening) with the following drugs: Aripiprazole, Risperidone, Ziprasidone, Clozapine, Chlorpromazine, Amitryptyline, Nefazodone, Trazodone, Buspirone, Pindolol, Penbutolol, Tertatolol, Alprenolol, Quetiapine
  • Investigations using PET or SPECT within 10 years prior to the inclusion

Sites / Locations

  • Medical University of Vienna, Dept. of Psychiatry and Psychotherapy

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ECT

Arm Description

Outcomes

Primary Outcome Measures

serotonin-1A receptor binding potential

Secondary Outcome Measures

Full Information

First Posted
June 16, 2009
Last Updated
November 15, 2011
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT00922064
Brief Title
Effects of Electroconvulsive Therapy (ECT) on Serotonin-1A Receptor Binding
Official Title
Effects of Electroconvulsive Therapy on Serotonin-1A Receptor Binding in Major Depression
Study Type
Interventional

2. Study Status

Record Verification Date
November 2011
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In treatment-resistant depression, electroconvulsive therapy (ECT) has been shown to effectively reduce depressive symptoms, though the underlying neurobiological mechanism is still unclear. The serotonergic system, and in particular the inhibitory serotonin-1A (5-HT1A) receptor, appears to be significantly involved in the effectiveness of ECT. The aim of the study is to assess the effects of ECT on the 5-HT1A receptor binding potential (BPND) and distribution in humans in vivo using positron emission tomography (PET) and the radioligand [carbonyl-11C]WAY-100635. 12 patients suffering from severe, therapy-resistant unipolar depression will undergo 3 PET scans, two of these scans taking place before the ECT treatment, consisting of 6-14 ECTs, the third scan taking place after the ECT treatment. This imaging study hypothesizes that upon completion of the ECT, the overall 5-HT1A receptor BPND in the brain of depressed patients will significantly change. This study would be the first to demonstrate an effect of electroconvulsive therapy on the 5-HT1A receptor binding in humans in vivo. Given the involvement of the 5-HT1A receptor in the pathophysiology of mood disorders, the present study would be an important step towards a better understanding of antidepressant treatment and treatment response. By comparing treatment effect and the underlying biological mechanism, the study might help to identify biomarkers that distinguish patients who are likely to benefit from ECT from patients who will rather be non-responders. Finally, by investigating the role of the 5-HT1A receptor in ECT, is highly discussed relevance for antidepressant action will be further elucidated and might prepare the ground for new therapeutic strategies.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unipolar Depression

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ECT
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
ECT
Intervention Description
ECT series consisting of 6 to 14 ECTs
Primary Outcome Measure Information:
Title
serotonin-1A receptor binding potential
Time Frame
2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female Age 18 - 65 years ICD-10 diagnosis of severe unipolar depression (ICD-10: F32.2, F32.3; F33.2, F33.3) A score of 23 or greater on the 17-item HAM-D Signed informed consent form Negative urine pregnancy test in women at the screening visit and at PET days Antidepressive and antipsychotic medication in a steady state for at least 10 days prior to inclusion Anesthesiological approval for ECT Exclusion Criteria: Concomitant major internistic or neurological illness Clinically relevant abnormalities on a general physical examination and routine laboratory screening Current substance abuse, addiction Current or past history of schizophrenia or schizoaffective disorder Exposure to artificial radiation as volunteer in clinical studies within 10 years prior to inclusion into the present study Previous treatments with electroconvulsive therapy Treatment (< 1 months before screening) with the following drugs: Aripiprazole, Risperidone, Ziprasidone, Clozapine, Chlorpromazine, Amitryptyline, Nefazodone, Trazodone, Buspirone, Pindolol, Penbutolol, Tertatolol, Alprenolol, Quetiapine Investigations using PET or SPECT within 10 years prior to the inclusion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard Frey, MD
Organizational Affiliation
Medical University of Vienna, Dept. of Psychiatry and Psychotherapy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of Vienna, Dept. of Psychiatry and Psychotherapy
City
Vienna
ZIP/Postal Code
1090
Country
Austria

12. IPD Sharing Statement

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Effects of Electroconvulsive Therapy (ECT) on Serotonin-1A Receptor Binding

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