Status:

Lead Sponsor:

No Sponsor

Collaborating Sponsors:

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Conditions:

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Eligibility:

All genders

Above 18+

Phase:

1/4

Participant Compensation:

n/a

Eligibility Criteria

Inclusion

    Exclusion

      Key Trial Info

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      Trial Type :

      Clinical Trial

      End Date :

      Estimated Enrollment :

      Patients enrolled

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      Study of the Efficacy and Safety of Initial Administration of 17 mg Vortioxetine Intravenously With 10 mg/Day Vortioxetine Orally in Patients With Major Depressive Disorder | DecenTrialz