Viewing Study NCT00236548



Ignite Creation Date: 2024-05-05 @ 12:05 PM
Last Modification Date: 2024-10-26 @ 9:20 AM
Study NCT ID: NCT00236548
Status: COMPLETED
Last Update Posted: 2011-05-18
First Post: 2005-10-07

Brief Title: Evaluation of the Usefulness to Doctors of the Risperdal Consta Treatment Guidebook Over a Three-month Period During Which Adult Patients With Schizophrenia or Schizoaffective Disorder Are Switching From Daily Doses or Risperidone Tablets to Long-acting Risperidone by Injection
Sponsor: Johnson Johnson Pharmaceutical Research Development LLC
Organization: Johnson Johnson Pharmaceutical Research Development LLC

Study Overview

Official Title: An Open-label Evaluation of the Utility of the RISPERDAL CONSTA Treatment Guidebook During Transition of Adult Patients With Schizophrenia or Schizoaffective Disorder to RISPERDAL CONSTA Risperidone Treatment Over Three Months in the Community Mental Health Center CMHC Setting
Status: COMPLETED
Status Verified Date: 2011-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess the usefulness of the Risperdal Consta Treatment Guidebook in helping the doctor switch the adult patient from taking risperidone tablets daily by mouth to taking long-acting risperidone by injection The study will also evaluate the effectiveness and safety of long-acting risperidone and its effect on patient satisfaction
Detailed Description: Many patients who take oral medication to treat schizophrenia or schizoaffective disorder have trouble taking their medication every day They may not want to take it or they may just forget Risperidone injections given once every 2 weeks are expected to be just as effective as risperidone tablets taken once a day The option of getting an injection every 2 weeks rather than taking a tablet every day may help patients keep to their medication administration schedule and could help to reduce the symptoms of their disease The study will assess the usefulness of the Risperdal Consta Treatment Guidebook in a Community Mental Health Center setting over a period of three months This Guidebook was designed to help doctors switch adult patients from oral risperidone tablets to long-acting risperidone given once every 2 weeks by injection During the study patients will continue to take oral risperidone for 2 weeks following initiation of risperidone injections which will be given every 2 weeks during a 12-week period Physical examinations and laboratory tests will be performed to test the safety of the risperidone injections Both the patient and the doctor will be asked questions about the usefulness of the guidebook and the effectiveness of the injections The objective of this study is to demonstrate the effectiveness of the Risperdal Consta Treatment Guidebook in switching patients with schizophrenia and schizoaffective disorder from daily oral risperidone to long-acting risperidone injections In addition safety evaluations are assessed throughout the study Risperidone oral tablets 2 to 6 milligrams per day for the first 2 weeks after initiation of long-acting risperidone injections long-acting risperidone injections are given in doses of 25 375 or 50 milligrams per 2 milliliter injection once every 2 weeks for 12 weeks

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None