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Randomized Double Blind Placebo Control Study in Patients With Schizophrenia (ROSES)

Primary Purpose

Schizophrenia, Schizoaffective Disorder, Psychosis Not Otherwise Specified

Status
Completed
Phase
Phase 2
Locations
Pakistan
Study Type
Interventional
Intervention
Ondansetron
Simvastatin
Placebo
Odansetron plus simvastatin
Sponsored by
Pakistan Institute of Living and Learning
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Anti inflammatory, Schizophrenia, Simvastatin, Ondansetron

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  1. Patients aged 18 to 65 years
  2. Patients will be recruited both from inpatients and outpatients.
  3. Diagnostic and Statistical Manual-IV (DSM-IV TR) diagnosis of schizophrenia, schizoaffective disorder, psychosis not otherwise specified or schizophreniform disorder
  4. Competent and willing to give informed consent
  5. Stable on medication 4 weeks prior to baseline
  6. No planned medication change
  7. Able to take oral medication and likely to complete the required evaluations
  8. Female participants of child bearing age must be willing to use adequate contraceptives for the duration of the study, and, willing to have a pregnancy test pre treatment and at ten weekly intervals while on study medication,
  9. Not planning to relocate in the next 12 months

Exclusion Criteria

  1. Relevant ICD 10 organic brain disease or neurological diagnoses (including ECG conduction abnormalities, neurological disorder, or an active seizure)
  2. Subjects who will meet the criteria for a DSM-IV TR diagnosis of alcohol or substance abuse (other than for nicotine) within the last month or the criteria for DSM-IV TR alcohol or substance dependence (other than for nicotine) within the last 6 months
  3. Any change of psychotropic medications within the previous 4 weeks
  4. Pregnant or lactating women and those of reproductive age without adequate contraception

Sites / Locations

  • Abbasi Shaheed Hospital
  • Dow university of Health Sciences
  • Karwan e hayat

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Active Comparator

Arm Label

Ondansetron

Simvastatin

Placebo

Odansetron Plus Simvastatin

Arm Description

ondansetron added to TAU Ondansetron will be administered in 8mg once daily dose

Simvastatin added to TAU Simvastatin 20mg taken as once daily dose

Placebo added to TAU

Ondansetron will be administered in 8mg once daily dose and Simvastatin 20mg taken as once daily dose

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

cognitive functioning
Full PANSS and positive syndrome subscale score Clinical Global Impression Functional outcome

Full Information

First Posted
May 17, 2012
Last Updated
November 8, 2014
Sponsor
Pakistan Institute of Living and Learning
Collaborators
Stanley Medical Research Institute, Dow University of Health Sciences, Karwan e Hayat, Abbasi Shaheed Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01602029
Brief Title
Randomized Double Blind Placebo Control Study in Patients With Schizophrenia
Acronym
ROSES
Official Title
Randomized Double Blind Placebo Controlled Study of Ondansetron and Simvastatis Added to Treatment as Usual in Patients With Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Completed
Study Start Date
August 2010 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pakistan Institute of Living and Learning
Collaborators
Stanley Medical Research Institute, Dow University of Health Sciences, Karwan e Hayat, Abbasi Shaheed Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder, Psychosis Not Otherwise Specified, Schizophreniform Disorder
Keywords
Anti inflammatory, Schizophrenia, Simvastatin, Ondansetron

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
303 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ondansetron
Arm Type
Active Comparator
Arm Description
ondansetron added to TAU Ondansetron will be administered in 8mg once daily dose
Arm Title
Simvastatin
Arm Type
Active Comparator
Arm Description
Simvastatin added to TAU Simvastatin 20mg taken as once daily dose
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo added to TAU
Arm Title
Odansetron Plus Simvastatin
Arm Type
Active Comparator
Arm Description
Ondansetron will be administered in 8mg once daily dose and Simvastatin 20mg taken as once daily dose
Intervention Type
Drug
Intervention Name(s)
Ondansetron
Intervention Description
ondansetron added to TAU Ondansetron will be administered in 8mg once daily dose
Intervention Type
Drug
Intervention Name(s)
Simvastatin
Intervention Description
Simvastatin added to TAU Simvastatin 20mg taken as once daily dose
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo added to TAU
Intervention Type
Drug
Intervention Name(s)
Odansetron plus simvastatin
Intervention Description
Ondansetron will be administered in 8mg once daily dose and Simvastatin 20mg taken as once daily dose
Primary Outcome Measure Information:
Title
Negative symptom severity
Description
Negative symptom severity as defined by negative syndrome subscale score on the Positive and Negative Syndrome Scale
Time Frame
6 months
Secondary Outcome Measure Information:
Title
cognitive functioning
Description
Full PANSS and positive syndrome subscale score Clinical Global Impression Functional outcome
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients aged 18 to 65 years Patients will be recruited both from inpatients and outpatients. Diagnostic and Statistical Manual-IV (DSM-IV TR) diagnosis of schizophrenia, schizoaffective disorder, psychosis not otherwise specified or schizophreniform disorder Competent and willing to give informed consent Stable on medication 4 weeks prior to baseline No planned medication change Able to take oral medication and likely to complete the required evaluations Female participants of child bearing age must be willing to use adequate contraceptives for the duration of the study, and, willing to have a pregnancy test pre treatment and at ten weekly intervals while on study medication, Not planning to relocate in the next 12 months Exclusion Criteria Relevant ICD 10 organic brain disease or neurological diagnoses (including ECG conduction abnormalities, neurological disorder, or an active seizure) Subjects who will meet the criteria for a DSM-IV TR diagnosis of alcohol or substance abuse (other than for nicotine) within the last month or the criteria for DSM-IV TR alcohol or substance dependence (other than for nicotine) within the last 6 months Any change of psychotropic medications within the previous 4 weeks Pregnant or lactating women and those of reproductive age without adequate contraception
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Imran Chaudhry, MD
Organizational Affiliation
University of Manchester
Official's Role
Principal Investigator
Facility Information:
Facility Name
Abbasi Shaheed Hospital
City
Karachi
State/Province
Sindh
Country
Pakistan
Facility Name
Dow university of Health Sciences
City
Karachi
State/Province
Sind
Country
Pakistan
Facility Name
Karwan e hayat
City
Karachi
Country
Pakistan

12. IPD Sharing Statement

Citations:
PubMed Identifier
23782463
Citation
Chaudhry IB, Husain N, Husain MO, Hallak J, Drake R, Kazmi A, Rahman Ru, Hamirani MM, Kiran T, Mehmood N, Stirling J, Dunn G, Deakin B. Ondansetron and simvastatin added to treatment as usual in patients with schizophrenia: study protocol for a randomized controlled trial. Trials. 2013 Apr 17;14:101. doi: 10.1186/1745-6215-14-101.
Results Reference
derived
Links:
URL
http://pill.org.pk
Description
Website of Pakistan Institute of Learning & Living

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Randomized Double Blind Placebo Control Study in Patients With Schizophrenia

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