Acute Efficacy and 6 Months Follow up After Electroconvulsive Therapy
Recruiting now
Conditions studied: Depressive Disorder
In brief
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.
Key facts
- Study ID
- NCT05388461
- Run by
- Haukeland University Hospital
- People needed
- 600
- Starts
- 2013-03-13
- Expected to finish
- 2028-12-01
- Last updated by the study team
- 2023-09-26
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- ECT performed on other indications than major depression.
- No consent to the register.
Where it is running
- Haukeland University Hospital — Bergen, Norway (enrolling)
- Stavanger University Hospital — Stavanger, Norway (enrolling)
Full record on ClinicalTrials.gov
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