Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE2
50 participants
INTERVENTIONAL
2010-02-28
2011-04-30
Brief Summary
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Detailed Description
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Overall, alleviation of clinical and neurological symptoms in EAE mice by MS14 explained the beneficial effects of traditionally used MS14 in MS patients, an effect which could also be investigated in other groups of psychological and neurological diseases. Additionally, there are anecdotal but unconfirmed reports for the effectiveness of MS14 in patients with schizophrenia. In this regard, we have decided to perform a randomized placebo-controlled study on the effect of MS14 on schizophrenia, to assess the safety and efficacy of this compound.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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treatment group
The treatment group receives Risperidone 2 mg per day in the beginning which is increased by 1 mg every day until reaching 4 mg/day; this regimen will be continued for three months. MS14 will be administered at an oral dose of 25-50 mg/kg/day in two divided doses for three months.
MS14
MS14 will be administered at an oral dose of 25-50 mg/kg/day in two divided doses for three months
Risperidone
The treatment group receives Risperidone 2 mg per day in the beginning which is increased by 1 mg every day until reaching 4 mg/day; this regimen will be continued for three months.
Control group
Receives the same dosage of Risperidone. Placebo is given to this group in same form and appearance as MS14 in the other arm of the study.
Risperidone
The treatment group receives Risperidone 2 mg per day in the beginning which is increased by 1 mg every day until reaching 4 mg/day; this regimen will be continued for three months.
Interventions
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MS14
MS14 will be administered at an oral dose of 25-50 mg/kg/day in two divided doses for three months
Risperidone
The treatment group receives Risperidone 2 mg per day in the beginning which is increased by 1 mg every day until reaching 4 mg/day; this regimen will be continued for three months.
Eligibility Criteria
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Inclusion Criteria
* Signing the consent form by either the patient or their guardian
* Proved diagnosis of schizophrenia through SCID structured interview
Exclusion Criteria
* Recent resistance to risperidone
* Contraindications of MS14 or risperidone administration
* Patients with residual or simple schizophrenia
* Age over 65 or under 18 years
18 Years
65 Years
ALL
No
Sponsors
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Farzan Institute
OTHER
Responsible Party
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Farzan Institute
Principal Investigators
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Seyed Vahid Shariat
Role: PRINCIPAL_INVESTIGATOR
Department of Psychiatry and Mental Health Research Center, Iran University of Medical Sciences
Locations
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Iran Psychiatric Training and Treatment Center
Tehran, Tehran Province, Iran
Countries
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Central Contacts
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Other Identifiers
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09123272376
Identifier Type: -
Identifier Source: org_study_id
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