CompletedNCT01192867
Official study titleA Phase III, Multi-Center, Randomized, 24 Week, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate Efficacy and Safety of RO4917838 in Stable Patients With Persistent, Predominant Negative Symptoms of Schizophrenia Treated With Antipsychotics Followed by a 28 Week, Double-Blind Treatment Period
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockSchizophreniaMedication studyAges 18+
- Countries
- United States, Australia, France, + 11 others
- Sponsor
- Hoffmann-La Roche
CompletedNCT01235520
What is this study about?Researchers compared RO4917838 and placebo to find out how the approaches affected psychotic symptoms in people with schizophrenia.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockSchizophreniaMedication studyAges 18+
- Countries
- United States, Australia, France, + 11 others
- Sponsor
- Hoffmann-La Roche
CompletedNCT03273439
Official study titleA Randomized, Double-blind Study of Repetitive Transcranial Magnetic Stimulation for Cognitive Deficits in Chronic Patients With Schizophrenia in a Chinese Han Population
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaDevice studyAges 18–60
- Countries
- Sponsor
- Suzhou Psychiatric Hospital
CompletedNCT00077727
Official study titleA Study of Galantamine HBr as an Adjunctive Treatment to Atypical Antipsychotic Medications in Outpatients With Schizophrenia and Associated Cognitive Deficits.
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18–55
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00253136
Official study titleRisperidone Depot (Microspheres) vs. Placebo in the Treatment of Subjects With Schizophrenia
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18–55
- Countries
- Sponsor
- Janssen, LP
CompletedNCT00249132
Official study titleRisperidone Versus Haloperidol Versus Placebo in the Treatment of Chronic Schizophrenia
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18–65
- Countries
- Sponsor
- Janssen, LP
CompletedNCT00246285
What is this study about?This study evaluated the safety and effectiveness of risperidone for people with schizophrenia.
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 13–17
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00538070
Official study titleThe Effects of Glycine Transport Inhibition on Brain Glycine Concentration
This study has finished and is no longer accepting participants.
Multiple locations, including BelmontSchizophreniaPlacebo comparisonAges 18–65
- Countries
- United States
- Sponsor
- Massachusetts General Hospital (Hospital / academic medical center)
CompletedNCT00111189
Official study titleA Randomized Double-blind Placebo-controlled Parallel Group Study Evaluating Paliperidone Palmitate in the Prevention of Recurrence in Patients With Schizophrenia. Placebo Consists of 20% Intralipid (200 mg/mL) Injectable Emulsion.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockSchizophreniaMedication studyAges 18–65
- Countries
- United States, Costa Rica, Mexico, + 6 others
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00240708
Official study titleA Parallel-Group Comparative Open-Label Study of Long-Acting Injectible Risperidone Versus Risperidone Tablets in Patients With Schizophrenia.
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 20+
- Countries
- Sponsor
- Janssen Pharmaceutical K.K.
CompletedNCT00210769
Official study titleOpen-label Extension of A Randomized, Double-Blind, Placebo- and Active-Controlled, Parallel-Group, Dose-Response Study to Evaluate the Efficacy and Safety of 2 Fixed Dosages of Extended Release OROS� Paliperidone (6 and 12 mg/Day) and Olanzapine (10 mg/Day), in Patients With Schizophrenia
This study has finished and is no longer accepting participants.
Location not clearly listedSchizophreniaMedication studyAges 18+
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT02019329
What is this study about?This study evaluated the safety of RO5545965 for people with schizophrenia.
This study has finished and is no longer accepting participants.
In GlendaleSchizophreniaMedication studyAges 18–60
- Countries
- United States
- Sponsor
- Hoffmann-La Roche