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

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Rupert Lanzenberger, Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT00922064
First received: June 16, 2009
Last updated: November 15, 2011
Last verified: November 2011

June 16, 2009
November 15, 2011
June 2009
September 2011   (final data collection date for primary outcome measure)
serotonin-1A receptor binding potential [ Time Frame: 2 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00922064 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Effects of Electroconvulsive Therapy (ECT) on Serotonin-1A Receptor Binding
Effects of Electroconvulsive Therapy on Serotonin-1A Receptor Binding in Major Depression

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.

Not Provided
Interventional
Phase 4
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Basic Science
Unipolar Depression
Procedure: ECT
ECT series consisting of 6 to 14 ECTs
Experimental: ECT
Intervention: Procedure: ECT
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
12
September 2011
September 2011   (final data collection date for primary outcome measure)

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
Both
18 Years to 60 Years
No
Contact information is only displayed when the study is recruiting subjects
Austria
 
NCT00922064
EKT-20090219 Version 1.3, MUW EC No. 556/2008
Yes
Rupert Lanzenberger, Medical University of Vienna
Medical University of Vienna
Not Provided
Principal Investigator: Richard Frey, MD Medical University of Vienna, Dept. of Psychiatry and Psychotherapy
Medical University of Vienna
November 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP