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Recruiting NCT05388461
Acute Efficacy and 6 Months Follow up After Electroconvulsive Therapy
Trial Parameters
Condition Depressive Disorder
Sponsor Haukeland University Hospital
Study Type OBSERVATIONAL
Phase N/A
Enrollment 600
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2013-03-13
Completion 2028-12
Interventions
electroconvulsive therapy
Brief Summary
The overall aim of the current project is to assess the acute and long term outcome of ECT (both patient and clinician rated) in a non-selected patient cohort from ordinary clinical activity, and to seek out factors predicting response and remission, side effects and relapse.
Eligibility Criteria
Inclusion Criteria: * Patients treated with ECT for major depression (F31.3-5, F32, F33) at Haukeland University Hospital or Stavanger University Hospital after 2013, * written consent to enrolment into the Regional Register for neurostimulation. Exclusion Criteria: * ECT performed on other indications than major depression. * No consent to the register.