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CompletedNCT00650429

Injected then oral ziprasidone for acute schizophrenia or schizoaffective symptoms

About this title

A Study of the Efficacy and Safety of Ziprasidone for the Treatment of Acute Exacerbation of Schizophrenia or Schizoaffective Disorder

Read the official source — NCT00650429
Medication studyAges 18–70Mexico
The study in practice

Understand this study

Who was this study for?

Listed age limits: 18 years to 70 years.

Listed locations
Monterrey and 3 more locationsSee all locations and recruitment
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Study clarity

Study information

Study start dateOctober 2003
Recruitment status
Completed
Enrollment listed in the registry
28
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
Mexico
Age range
From 18 Years to 70 Years
Official registry ID
NCT00650429
Official title
Show the full official title

Ziprasidone Intramuscular/Oral In The Treatment Of Acute Exacerbation Of Schizophrenia Or Schizoaffective Disorder: A Six-Week Open Administration Study

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Recruitment & locations

Completed

Monterrey · DF · Mexico City

1 more locations
  • Mexico D F
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

Did this study involve medication?

Yes. The study involved medication, including Ziprasidone.

Who was this study for?

Listed age limits: 18 years to 70 years.

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