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Clinical Trials/NCT06661616
NCT06661616
Completed
Not Applicable

Cognitive Effects Associated With Hippocampal Neurogenesis Induced by Electroconvulsive Therapy in the Treatment of Depression

Centre Hospitalier St Anne1 site in 1 country87 target enrollmentJune 6, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Major Depressive Disorder (MDD)
Sponsor
Centre Hospitalier St Anne
Enrollment
87
Locations
1
Primary Endpoint
Correlation between increased hippocampal volume and post-ECT retrograde amnesia
Status
Completed
Last Updated
last year

Overview

Brief Summary

Electroconvulsive therapy (ECT) is the treatment of choice for drug-resistant depression (30% of patients), or when there is a short-term risk to the patient's life. Despite its robust efficacy and rapid onset of action, its use is limited both by the limited range of treatment available and by the cognitive effects sometimes induced. The present study focuses on the links between the efficacy of ECT, its cognitive effects and the formation of new neurons in the hippocampus (hippocampal neurogenesis) associated with this treatment.

Registry
clinicaltrials.gov
Start Date
June 6, 2018
End Date
May 14, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Centre Hospitalier St Anne
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Study population: depressed subjects treated with ECT
  • Male or female over 18 years of age
  • Hospitalised at the Centre Hospitalier Sainte-Anne
  • Suffering from a unipolar or bipolar major depressive episode, according to DSM5 criteria
  • Indication for ECT treatment
  • Patient has given informed written consent
  • Beneficiary of a social security scheme
  • Control population: depressed subjects treated without ECT
  • Male or female over 18 years of age
  • Hospitalised at the Centre Hospitalier Sainte-Anne

Exclusion Criteria

  • Study population: depressed subjects with ECT
  • Psychiatric comorbidity: schizophrenia, pervasive developmental disorder, dependence on a substance other than tobacco
  • Neurological comorbidity: Parkinson's disease, dementia
  • ECT treatment in the 6 months prior to inclusion
  • Compulsory care
  • Protected adults, persons under court protection measures
  • Persons deprived of liberty by judicial or administrative decision;
  • Refusal of consent to ECT treatment
  • Contraindications to ECT (HTIC, recent history of stroke, severe uncontrolled arterial hypertension, contraindication to anaesthesia)
  • Contraindications to MRI (patients with metal prostheses, claustrophobia)

Outcomes

Primary Outcomes

Correlation between increased hippocampal volume and post-ECT retrograde amnesia

Time Frame: After a course of ECT, up to 3 months

Study Sites (1)

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