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A Comparative Trial of TMS Approaches to Treating Depression

A Comparative Trial of TMS Approaches to Treating Depression

Status
Withdrawn
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01906905
Enrollment
0
Registered
2013-07-24
Start date
2013-06-30
Completion date
2013-12-31
Last updated
2023-04-03

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

Conditions

Depression

Brief summary

Trancranial Magnetic Stimulation (TMS) is a non-drug and non-invasive treatment for depression and has been investigated for the treatment of psychiatric illness for over 15 years. There is now established evidence indicating TMS is an effective treatment for depression. However, the effectiveness of TMS varies between people, thus requiring further research to investigate its optimal application. Investigators want to compare the effectiveness of different forms of TMS, given with differing stimulation settings to the right or left side of the brain that has been associated with depression. This could potentially help clinicians in the future to improve the prescription of TMS as a treatment for depression.

Interventions

DEVICETranscranial Magnetic Stimulation

Sponsors

The University of New South Wales
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

1. Age ≥18 years. 2. DSM-IV diagnosis of current Major Depressive Episode. 3. MADRS score of 20 or more. 4. Able to give informed consent.

Exclusion criteria

1. DSM-IV psychotic disorder. 2. Drug or alcohol abuse or dependence (preceding 3 months). 3. Inadequate response to ECT (current episode of depression). 4. Rapid clinical response required, e.g. high suicide risk. 5. Significant neurological disorder, which may pose increased risks with TMS, e.g., epilepsy. 6. Metal in the cranium, skull defects, pacemaker, cochlear implant, medication pump or other electronic device. 7. Pregnancy.

Design outcomes

Primary

MeasureTime frame
Montgomery-Åsberg Depression Rating Scale(MADRS)Participants will be assessed for changes for duration of trial, an expected average of 6 weeks.

Countries

Australia

Outcome results

None listed

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