Geodon in Weight Loss Study for Bipolar Disorders
NCT00472641 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 25
Last updated 2017-05-09
Summary
This research study is designed to determine if replacing your current antipsychotic and/or mood stabilizer with ziprasidone (Geodon) will impact weight. This research is being conducted because Geodon has a documented effect on mood. Additionally, we believe Geodon to be an effective medication for overweight or obese patients with bipolar disorder. There will be approximately 25 patients enrolled in this study.
Conditions
- Bipolar Disorder
Interventions
- DRUG
-
Ziprasidone/Geodon
Ziprasidone/Geodon
Sponsors & Collaborators
-
Pfizer
collaborator INDUSTRY -
Stanford University
lead OTHER
Principal Investigators
-
Terence Arthur Ketter · Stanford University
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-01-31
- Primary Completion
- 2009-12-31
- Completion
- 2009-12-31
Countries
- United States
Study Locations
Related Clinical Trials
-
Study Comparing the Affect of Bifeprunox Vs Olanzapine on Weight During the Treatment of Outpatients With Schizophrenia.
NCT00380224 · Status: COMPLETED · Phase: PHASE3
- Schizophrenia
-
Study Comparing Bifeprunox to Risperidone in Treatment of Outpatients With Schizophrenia With Weight as Primary Endpoint
NCT00366704 · Status: TERMINATED · Phase: PHASE3
- Schizophrenia
-
Compare the Effects of Bifeprunox and Quetiapine on Weight Changes in Stable Schizophrenic Patients
NCT00396214 · Status: TERMINATED · Phase: PHASE3
- Schizophrenia
-
Progressively Decreasing Titration Schedules of Bifeprunox in Subjects With Schizophrenia or Bipolar Disorder
NCT00139919 · Status: COMPLETED · Phase: PHASE2
- Schizophrenia
- Schizoaffective Disorder
- Bipolar Disorder
-
Switch Study of Existing Atypical Antipsychotics to Bifeprunox
NCT00347425 · Status: COMPLETED · Phase: PHASE3
- Schizophrenia and Schizoaffective Disorder
More Related Trials
-
PK Effects of Bifeprunox & Valproate in Bipolar I
NCT00141505 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy of Bifeprunox in Patients With Schizophrenia
NCT00704509 ·Status: TERMINATED ·Phase: PHASE3
-
Twice Daily Titration Study of Bifeprunox in Subjects With Schizophrenia
NCT00139906 ·Status: COMPLETED ·Phase: PHASE2
-
To Evaluate the Impact of Treatment Interruption on Re-initiation of Bifeprunox
NCT00141479 ·Status: COMPLETED ·Phase: PHASE2
-
Study Evaluating Bifeprunox in Bipolar Depression
NCT00134459 ·Status: COMPLETED ·Phase: PHASE3
-
Open Label Extension Study of Bifeprunox
NCT00366171 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate Efficacy and Safety of Bitopertin in Participants With Persistent, Predominant Negative Symptoms of Schizophrenia
NCT01192880 ·Status: COMPLETED ·Phase: PHASE3
-
Study Evaluating Bifeprunox in Patients With Schizophrenia.
NCT00366327 ·Status: TERMINATED ·Phase: PHASE3
-
Bifeprunox in the Treatment of Schizophrenia
NCT00193713 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy of Bifeprunox in Patients With Schizophrenia
NCT00658645 ·Status: TERMINATED ·Phase: PHASE3
-
Study Evaluating Bifeprunox in Bipolar Depression
NCT00245973 ·Status: COMPLETED ·Phase: PHASE3
-
Bifeprunox in the Treatment of Schizophrenia
NCT00193687 ·Status: COMPLETED ·Phase: PHASE3
-
Bifeprunox Extension to Extension Study in Patients With Schizophrenia
NCT00861497 ·Status: TERMINATED ·Phase: PHASE3
-
A Study of RO4917838 (Bitopertin) in Patients With Persistent, Predominant Negative Symptoms of Schizophrenia (WN25309)
NCT01192906 ·Status: COMPLETED ·Phase: PHASE3
-
Patient-reported Outcomes in the Treatment of Schizophrenia
NCT00230828 ·Status: COMPLETED ·Phase: PHASE3
-
Treatment of Elderly Subjects With Psychosis and Behavioral Disturbances Associated With Dementia of the Alzheimer's Type
NCT00160147 ·Status: TERMINATED ·Phase: PHASE3
-
Pharmacokinetic Study of VHX-896 and Iloperidone Tablets Under Steady-State Conditions
NCT06494397 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of RO4917838 (Bitopertin) in Patients With Sub-optimally Controlled Symptoms of Schizophrenia (WN25305)
NCT01235559 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of RO4917838 (Bitopertin) in Patients With Sub-optimally Controlled Symptoms of Schizophrenia (WN25306)
NCT01235585 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy, Safety, and Tolerability of Brexpiprazole (OPC-34712) as Maintenance Treatment in Adults With Schizophrenia
NCT01668797 ·Status: COMPLETED ·Phase: PHASE3
-
Bio-equivalence Study Between SAPHRIS and Asenapine
NCT01948024 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study in Healthy Men and Women to Compare Two Pharmaceutical Formulations of Flupentixol/Melitracen (Deanxit®)
NCT02179931 ·Status: COMPLETED ·Phase: PHASE1
-
Study Evaluating the Tolerability of Bifeprunox in Healthy Subjects
NCT00581451 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study to Compare Two Formulations of Deanxit®
NCT03472651 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Pimavanserin 34 mg Capsule
NCT06450184 ·Status: COMPLETED ·Phase: PHASE1