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An Open, Multicenter, Non-Comparative Study To Assess The Efficacy And Tolerability Of Intramuscular Ziprasidone Followed By Oral Ziprasidone In Patients With Acute Psychosis

NCT00644800 Phase 4 COMPLETED

To assess the efficacy, safety, and tolerability of intramuscular ziprasidone in the treatment of the acute exacerbation of non-organic psychosis of any etiology, including schizophrenia, acute mania, delusional disorder and others.

Details

Lead sponsorPfizer's Upjohn has merged with Mylan to form Viatris Inc.
PhasePhase 4
StatusCOMPLETED
Enrolment89
Start date2003-07
Completion2004-05

Conditions

Interventions

Primary outcomes

Countries

Brazil