WithdrawnN/Aketamine

Ketamine and Scopolamine Infusions for Treatment-resistant Major Depressive Disorder

Sponsored by Massachusetts General Hospital

NCT ID
NCT01613820
Start Date
2015-09
Est. Completion
2017-02

About This Study

Ketamine infusions resulted in an acute reduction in global depression scores and in severity of suicidal ideation. Scopolamine infusions produced also a significant improvement in depression that was sustained over time. We therefore plan to investigate the feasibility and efficacy of open-label repeated intravenous administration of ketamine and scopolamine combined in this population of severely depressed, treatment-resistant patients. The results from this study could lead to the development of new strategies for the treatment of patients with TRD.

Conditions Studied

Major Depressive Disorder

Interventions

  • Ketamine
  • Scopolamine

Eligibility

Age:18 Years - 65 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Outpatients with sever treatment-resistant depression
* Currently depressed
* Currently under regular psychiatric care
* On an aggressive antidepressant regimen, stable for 4 weeks

Exclusion Criteria:

* No history of other major psychiatric illnesses, including bipolar disorder
* No history of psychosis
* No history of drug abuse
* No major medical illness or unstable medical condition.

Study Locations (1)

Depression Clinical and Reseach Program - MGH
Boston, Massachusetts, United States

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source