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Randomized Double Blind Placebo Control Study in Patients with Schizophrenia

Phase 2
Completed
Conditions
Schizophrenia
Schizoaffective Disorder
Psychosis Not Otherwise Specified
Schizophreniform Disorder
Interventions
Registration Number
NCT01602029
Lead Sponsor
Pakistan Institute of Living and Learning
Brief Summary

Negative symptoms and cognitive deficits are two partially-related features of schizophrenia which have a major negative impact on social function and objective quality of life. Standard drug treatments have little impact on either and arguably no effect on primary negative symptoms. Social dysfunction has major economic consequences in both the developed and developing world. There is evidence that anti-inflammatory treatment may have beneficial effects in patients with schizophrenia.

Detailed Description

Negative symptoms and cognitive deficits are two partially-related features of schizophrenia which have a major negative impact on social function and objective quality of life. Evidence indicates that anti-inflammatory treatment may have beneficial effects in schizophrenia. From our preliminary randomised double-blind placebo-controlled clinical trial in Pakistan and Brazil, it is indicated that addition of minocycline (an antibiotic and anti-inflammatory drug) for one year to treatment as usual (TAU) reduced negative symptoms and improved some cognitive measures (Chaudhry et al 2009).

Statins are primarily HMG-CoA reductase inhibitors also anti-inflammatory agents and known to decrease C-reactive protein (CRP). Higher levels of CRP (\>0.50 mg/dl) are associated with marked negative symptoms and higher total PANSS scores in patients with schizophrenia. (Fan et al 2007)

Ondansetron, a selective 5-hydroxytryptamine-3 antagonist, is quite commonly used as an antiemetic in cancer patients (Marty et al 1990). There are several small trials suggesting that ondansetron as an adjunct to antipsychotics is effective in improving negative symptoms and memory in patients suffering from schizophrenia (Ahkonzadeh et al 2009, Levkovitz et al 2005 and Zhang et al 2006).

The Primary objective of this study is addition of ondansetron and /or simvastatin to TAU for patients with schizophrenia will result in improvement in negative symptoms

The Secondary objectives include:

* improvement in positive or other symptoms

* social functioning

* cognitive functions

* additive effects of ondansetron and simvastatin

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
303
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboPlacebo added to TAU
SimvastatinSimvastatinSimvastatin added to TAU Simvastatin 20mg taken as once daily dose
Odansetron Plus SimvastatinOdansetron plus simvastatinOndansetron will be administered in 8mg once daily dose and Simvastatin 20mg taken as once daily dose
OndansetronOndansetronondansetron added to TAU Ondansetron will be administered in 8mg once daily dose
Primary Outcome Measures
NameTimeMethod
Negative symptom severity6 months

Negative symptom severity as defined by negative syndrome subscale score on the Positive and Negative Syndrome Scale

Secondary Outcome Measures
NameTimeMethod
cognitive functioning6 months

1. Full PANSS and positive syndrome subscale score

2. Clinical Global Impression

3. Functional outcome

Trial Locations

Locations (3)

Dow university of Health Sciences

🇵🇰

Karachi, Sind, Pakistan

Karwan e hayat

🇵🇰

Karachi, Pakistan

Abbasi Shaheed Hospital

🇵🇰

Karachi, Sindh, Pakistan

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