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Repetitive transcranial magnetic stimulation in the treatment of depression.

Right parietal inhibition with rTMS in the treatment of depression.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23836
Enrollment
40
Registered
2005-09-05
Start date
2004-05-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

depression

Interventions

REPETITIVE TRANSCRANIAL MAGNETIC STIMULATION daily on 10 consecutive weekdays (five sessions per week), during 20 minutes per session.

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: In and outpatients aged between 16 and 65 who met DSM-IV criteria for major depressive episode, and who had a score of 25 or higher on the 10-item Montgomery Asberg Depression Rating Scale (MADRS) were included.

Exclusion criteria

Exclusion criteria: Exclusion criteria were a history of epilepsy and any other medical disorder that should preclude the administration of rTMS. Only SSRI's, Mirtazapine and Promethazine as psychotropic medication was accepted if the dosage of antidepressive medication had not been changed for 6 weeks, and if the dosage of Promethazine had not been changed for 2 weeks prior to inclusion. Antidepressive medication had to remain stable during the 14 weeks of the study. Furthermore: schizofrenic disorder, a piece if metal in the brain, pacemaker and left-handed patients.

Design outcomes

Primary

MeasureTime frame
Depression.

Secondary

MeasureTime frame
1. Changes in anxiety; 2. Autonomic changes; 3. Changes in the emotioneal attention, in the emotional memory en in de emotional recognition; 4. Biochemical changes; 5. Changes in the EEG.

Contacts

Public ContactJ. Riet, van der

St. Lucas Andreas Hospital, Department of Psychiatry, Jan Tooropstraat 164

+31 (0)20 5108562

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)