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Trials / Recruiting

RecruitingNCT05388461

Acute Efficacy and 6 Months Follow up After Electroconvulsive Therapy

Acute Efficacy and 6 Months Follow up After Electroconvulsive Therapy for Severe or Treatment Resistant Depression - Predictors of Response, Side Effects, and Relapse

Status
Recruiting
Phase
Study type
Observational
Enrollment
600 (estimated)
Sponsor
Haukeland University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERelectroconvulsive therapyelectroconvulsive therapy

Timeline

Start date
2013-03-13
Primary completion
2028-12-01
Completion
2028-12-01
First posted
2022-05-24
Last updated
2023-09-26

Locations

2 sites across 1 country: Norway

Source: ClinicalTrials.gov record NCT05388461. Inclusion in this directory is not an endorsement.