Status:
COMPLETED
Maintenance NeuroStar Transcranial Magnetic Stimulation (TMS) in Patients With Major Depressive Disorder
Lead Sponsor:
Neuronetics
Conditions:
Major Depressive Disorder
Eligibility:
All Genders
18-70 years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate the efficacy of scheduled maintenance Transcranial Magnetic Stimulation (TMS) treatment compared to on-demand TMS treatment for symptomatic worsening in patien...
Detailed Description
This is a 12-month maintenance treatment study for patients who have responded to a 6 week course of acute TMS treatment for major depressive disorder (MDD). The study will seek to assess the change i...
Eligibility Criteria
Inclusion
- Primary diagnosis by DSM-IV criteria for Major Depressive Episode, single episode or recurrent course of illness, with the additional stipulation of a duration for this episode of ≥ 4 weeks and CGI-S ≥ 4.
- Duration of current episode of depression ≤ 3 years (the definition of an episode is demarcated by a period of ≥ 2 months when the patient did not meet full criteria for the DSM-IV definition of Major Depressive Episode.
- Capable and willing to provide informed consent.
- Signed HIPAA authorization.
- Able to adhere with the treatment schedule, and withdrawal of ongoing pharmacotherapy.
- If currently taking antidepressant pharmacotherapy, must be clinically appropriate to discontinue treatment with those agents.
Exclusion
- Investigators, site personnel directly affiliated with this study, and their immediate families (immediate family is defined as a spouse, parent, child or sibling, whether by birth or legal adoption).
- Individuals diagnosed by the Investigator with the following conditions (current unless otherwise stated):
- Depression secondary to a general medical condition, or substance- induced;
- Seasonal pattern of depression as defined by DSM-IV;
- History of substance abuse or dependence within the past year except nicotine and caffeine);
- Any psychotic disorder (lifetime), including schizoaffective disorder, or major depression with psychotic features in this or previous episodes;
- Bipolar disorder;
- Eating disorder (current or within the past year);
- Obsessive compulsive disorder (lifetime); or
- Post-traumatic stress disorder (current or within the past year).
- An Axis II Personality Disorder, which in the judgment of the Investigator may hinder the patient in completing the procedures required by the study protocol.
- Individuals with a clinically defined neurological disorder or insult including, but not limited to:
- Any condition likely to be associated with increased intracranial pressure;
- Space occupying brain lesion;
- History of cerebrovascular accident;
- Transient ischemic attack within two years;
- Cerebral aneurysm;
- Dementia;
- Parkinson's disease;
- Huntington's chorea;
- Multiple sclerosis.
- Increased risk of seizure for any reason, including but not limited to prior diagnosis of increased intracranial pressure (such as after large infarctions or trauma), or history of significant head trauma with loss of consciousness for ≥ 5 minutes.
- History of treatment with Vagus Nerve Stimulation.
- Cardiac pacemakers, implanted medication pumps, intracardiac lines, or acute, unstable cardiac disease.
Key Trial Info
Start Date :
August 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2014
Estimated Enrollment :
67 Patients enrolled
Trial Details
Trial ID
NCT01415154
Start Date
August 1 2011
End Date
July 1 2014
Last Update
March 4 2025
Active Locations (6)
Enter a location and click search to find clinical trials sorted by distance.
1
Rush University Medical Center
Chicago, Illinois, United States, 60612
2
Sheppard Pratt Health System
Baltimore, Maryland, United States, 21285
3
Premier Psychiatric Group, L.L.C.
Lincoln, Nebraska, United States, 68526
4
Butler Hospital
Providence, Rhode Island, United States, 02906