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Clinical Trial 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.


Clinical Trial Description

Patients reffered to electroconvulsive ECT are (after written consent) enroled in a research registry. Based on (clinician and patient rated) measures of depressive symptoms and overall cognitive function, the short and long-term (6 months) efficacy of ECT will be described, and factors predicting response and relapse identified. The duration of possible cognitive impairment and factors predicting cognitive outcome will be examined. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05388461
Study type Observational [Patient Registry]
Source Haukeland University Hospital
Contact Ute Kessler, PhD
Email ute.kessler@helse-bergen.no
Status Recruiting
Phase
Start date March 13, 2013
Completion date December 2028

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