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Somatosensory Processing in Depression

L

Ludwig Maximilian University of Munich

Status and phase

Withdrawn
Phase 4

Conditions

Depression

Treatments

Procedure: simultaneous EEG/fMRI
Device: fMRI

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00386893
2005-003752-35
ESC_03082005

Details and patient eligibility

About

Aim of this study is to investigate neuronal differences (EEG/evoked potentials; functional MRI) between patients with major depression and healthy controls concerning brain activity after acute pain as well as changes of pain related brain activity during treatment with escitalopram.

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Psychiatric in or outpatients with acute depressive episode
  • Indication for pharmacological treatment

Exclusion criteria

  • Acute suicidal tendency
  • Neurological or severe somatic disorders
  • Women during pregnancy or lactation

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Treatment as usual
Other group
Description:
simultaneous EEG/fMRI
Treatment:
Device: fMRI
Procedure: simultaneous EEG/fMRI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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