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CompletedNCT00391222

Long-acting risperidone to prevent mood episodes in bipolarity type I

About this title

A Study to Evaluate the Efficacy and Safety of Risperidone for the Prevention of Mood Episodes in the Treatment of Patients With Bipolar I Disorder

Read the official source — NCT00391222
Medication studyAges 18–65Multiple countries
The study in practice

Understand this study

Who was this study for?

Listed age limits: 18 years to 65 years.

Listed locations
Baoding and 62 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateNovember 2006
Recruitment status
Completed
Enrollment listed in the registry
585
Sponsor
Janssen Pharmaceutica N.V., Belgium
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
China, Colombia, Germany, ...
Age range
From 18 Years to 65 Years
Official registry ID
NCT00391222
Official title
Show the full official title

A Randomized, Double Blind, Placebo and Active Controlled Parallel Group Study to Evaluate the Efficacy and Safety of Risperidone Long-acting Injectable (LAI) for the Prevention of Mood Episodes in the Treatment of Subjects With Bipolar I Disorder

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Recruitment & locations

Completed

Baoding, China · Beijing, China · Guangzhou, China

61 more locations
  • Nanjing, China
  • Shanghai, China
  • Suozhou, China
  • Wuhan, China
  • Barranquilla Atlantico, Colombia
  • Bello Antioquia, Colombia
  • Bogotá, Colombia
  • Bogotá S/N, Colombia
  • Medellin Antioquia, Colombia
  • Pereira Risaralda, Colombia
  • Freiburg im Breisgau, Germany
  • Hildesheim, Germany
  • Oranienburg, Germany
  • Athens, Greece
  • Ahmedabad, India
  • Bangalore, India
  • Chennai, India
  • Hyderabad, India
  • Ludhiana, India
  • Mangalore, India
  • Mumbai, India
  • New Delhi, India
  • Pune, India
  • Varanasi, India
  • Jakarta, Indonesia
  • Amman, Jordan
  • Beirut, Lebanon
  • Johor Bahru, Malaysia
  • Kuala Lumpur, Malaysia
  • Mexico City, Mexico
  • Mérida, Mexico
  • Monterrey, Mexico
  • Puebla City, Mexico
  • Tabasco, Mexico
  • Tampico, Mexico
  • Zapopan, Mexico
  • Lima, Peru
  • Lima Lima, Peru
  • Iloilo City, Philippines
  • Mandaluyong, Philippines
  • Mandaue City, Philippines
  • Arkhangelsky District, Russia
  • Chelyabinsk, Russia
  • Izhevsk, Russia
  • Kazan’, Russia
  • Moscow, Russia
  • Moscow Region, Russia
  • Nizny Novgorod, Russia
  • Orenburg, Russia
  • Saint Petersburg, Russia
  • Saratov, Russia
  • Stavropol Na, Russia
  • Tomsk Na, Russia
  • Voronezh, Russia
  • Bloemfontein, South Africa
  • Cape Town, South Africa
  • Durban, South Africa
  • Pretoria, South Africa
  • Tainan, Taiwan
  • Taipei, Taiwan
  • Russia
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Janssen Pharmaceutica N.V., Belgium.

Did this study involve medication?

Yes. The study involved medication, including Olanzapine, Placebo and Risperidone Long Acting Injectable (LAI).

Who was this study for?

Listed age limits: 18 years to 65 years.

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