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REPETITIVE TRANSCRANIAL MAGNETIC STIMULATION IN the Treatment of DEPRESSION

Right Parietal Inhibition With rTMS in the Treatment of Depression

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00220610
Enrollment
40
Registered
2005-09-22
Start date
2004-05-31
Completion date
2006-12-31
Last updated
2005-09-22

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

Conditions

Depression

Brief summary

Subjects received rTMS daily on 10 consecutive weekdays (five sessions per week), during 20 minutes per session.During the rTMS session, the coil was centered flat over the right parietal cortex. We follow the patient during 12 weeks after the 2 weeks of tms (follow-up period) to measure the depression with different rating scales. We hypothesized that rTMS has a positive effect in the treatment of depression

Interventions

DEVICETranscranial magnetic stimulation

Sponsors

St. Lucas Andreas Ziekenhuis Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
16 Years to 65 Years
Healthy volunteers
No

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

* 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: schizophrenic disorder, a piece if metal in the brain, pacemaker and left-handed patients.

Design outcomes

Primary

MeasureTime frame
To determine the depression (and so the effect of the treatment)we use the 10-item Montgomery Asberg Depression Rating Scale (MADRS)and we measure before tms (T=0), at week 1 (T=1), at week 2 (T=2), at week 4 (T=3), at week 8 (T=4), at week 14 (T=5)
Besides the MADRS we use the BDI (Beck depression Inventory, the Hamillton deppression and anxiety scale)

Secondary

MeasureTime frame
-.changes in the emotioneal attention, in the emotional memory en in de emotional recognition.
-.Biochemical changes
-Changes in anxiety
>> measured before tms and after (at T=0 and T=2)
-.Changes in the EEG
-.Autonomic changes

Countries

Netherlands

Contacts

Primary ContactJudith van der Riet, Drs.
j.vanderriet@slaz.nl0031-20-5108562

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026