Acute Efficacy and 6 Months Follow up After Electroconvulsive Therapy
Recruiting · NCT05388461 · Observational (researchers observe without assigning treatment) · Lead sponsor: Haukeland University Hospital
View the official record on ClinicalTrials.gov →Interventions studied
electroconvulsive therapy
What this trial is about
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.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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.
Where it is running
2 locations listed.
- Haukeland University Hospital - Bergen, Norway
- Stavanger University Hospital - Stavanger, Norway