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TerminatedNCT00946985

28-30 Month Study Comparing Paliperidone Palmitate With Oral Risperidone for Treating Adults Diagnosed With Schizophrenia Within the Past 5 Years

Medication studyAges 18–35Multiple countries
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 35 years.

Listed locations
Little Rock and 71 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 dateJune 2009
Recruitment status
Terminated
Enrollment listed in the registry
163
Sponsor
Ortho-McNeil Janssen Scientific Affairs, LLC
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
United States, Canada, Brazil, ...
Age range
From 18 Years to 35 Years
Official registry ID
NCT00946985
Official title
Show the full official title

A Prospective, Randomized, Active-controlled, Rater-blinded Study of the Prevention of Relapse Comparing Paliperidone Palmitate With Oral Risperidone in Adults With Recently-Diagnosed Schizophrenia Who Are at High Risk of Relapse

Questions about this study?

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Recruitment & locations

Terminated

Little Rock, United States · Garden Grove, United States · San Diego, United States

71 more locations
  • Washington D.C., United States
  • Kissimmee, United States
  • Tampa, United States
  • Chicago, United States
  • Hoffman Estates, United States
  • Kingsport, United States
  • Lake Charles, United States
  • Shreveport, United States
  • Pittsfield, United States
  • Minneapolis, United States
  • Flowood, United States
  • Creve Coeur, United States
  • St Louis, United States
  • Omaha, United States
  • Brooklyn, United States
  • Middleburg Heights, United States
  • Arlington, United States
  • Austin, United States
  • Irving, United States
  • Portsmount, United States
  • Curitiba, Brazil
  • Salvador, Brazil
  • São Paulo, Brazil
  • Kazanlak, Bulgaria
  • Pleven, Bulgaria
  • Radnevo, Bulgaria
  • Calgary, Canada
  • Halifax, Canada
  • Greater Sudbury, Canada
  • Montreal, Canada
  • Québec, Canada
  • Baoding, China
  • Beijing, China
  • Changsha, China
  • Guangzhou, China
  • Kunming, China
  • Shanghai, China
  • Wuhan, China
  • Xi'an, China
  • Bogotá, Colombia
  • Kutná Hora, Czechia
  • Olomouc, Czechia
  • Prague, Czechia
  • Strakonice, Czechia
  • Ahmedabad, India
  • Aurangabad, India
  • Calicut, India
  • Hyderabad, India
  • Jaipur, India
  • Lucknow Gpo, India
  • Mangalore, India
  • Pune, India
  • Varanasi, India
  • Johor Bahru, Malaysia
  • Kuala Lumpur, Malaysia
  • Moscow, Russia
  • Nizny Novgorod, Russia
  • Saint Petersburg, Russia
  • Samara, Russia
  • Yaroslavl, Russia
  • Gwangju, South Korea
  • Gyeonggi-do, South Korea
  • Jeonju, South Korea
  • Seoul, South Korea
  • Kharkiv, Ukraine
  • Kherson, Ukraine
  • Kiev, Ukraine
  • Odesa, Ukraine
  • Simferopol, Ukraine
  • Czechia
  • Russia

A listed location does not confirm current availability.

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Ortho-McNeil Janssen Scientific Affairs, LLC.

Does this study involve medication?

Yes. The study involves medication, including paliperidone palmitate and oral risperidone.

Who can participate?

Listed age limits: 18 years to 35 years.

Is this study still recruiting?

The registry lists this study as terminated.

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