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TerminatedNCT03643159

A Trial to Measure the Difference in All-cause Hospitalizations for Participants Who Are Using Abilify MyCite Versus Virtual Matched Controls in Adults With Schizophrenia, Bipolarity type I, and Major Depressive Disorder

Medication studyAges 18–63United StatesDepression
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 63 years.

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

What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: June 28, 2018
Recruitment status
Terminated
Enrollment listed in the registry
2
Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
COMBINATION_PRODUCT, Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
From 18 Years to 63 Years
Official registry ID
NCT03643159
Official title
Show the full official title

A Multicenter, 180-day Pragmatic Clinical Trial to Measure the Difference in All-cause Hospitalizations for Patients Who Are Using Abilify MyCite Versus Virtual Matched Controls in Adults With Schizophrenia, Bipolar 1 Disorder, and Major Depressive Disorder

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Recruitment & locations

Terminated

Santa Rosa · Decatur · Smyrna

2 more locations
  • Las Vegas
  • Fairlawn

A listed location does not confirm current availability.

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Otsuka Pharmaceutical Development & Commercialization, Inc., a pharmaceutical company.

Does this study involve medication?

Yes. The study involves medication, including Aripiprazole or other oral antipsychotics.

Who can participate?

Listed age limits: 18 years to 63 years.

Is this study still recruiting?

The registry lists this study as terminated.

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