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Adjunctive Selective Estrogen Receptor Modulators on Negative and Cognitive Symptoms of Schizophrenia in Women

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Raloxifene Hydrochloride
Placebo
Sponsored by
Shanghai Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring negtive symptoms, cognitive function

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Outpatient or inpatient, aged more than 45 years, postmenopausal female (menopause for more than one year)
  2. International Classification of Diseases, Tenth Revision, diagnosis of schizophrenia
  3. Continue to receive antipsychotic clozapine for more than 2 years with a stable dose of at least one month
  4. Negative symptoms scale >20 in PANSS, and a score of 4 (moderate) or more on one or more of N1-N7, and within two weeks before intervention, the total score of negative symptom factors improved by no more than 10%
  5. Able to give informed consent

Exclusion Criteria:

  1. Participating in other clinical studies
  2. Previous use of raloxifene intolerable
  3. Hormone related endocrine disease
  4. Acute liver disease
  5. thrombotic disease
  6. Estrogen dependent tumor
  7. Hyperthyreosis
  8. Severe cardiac dysfunction or renal disease
  9. Diabetes mellitus
  10. Abnormal uterine bleeding or cerebrovascular accident
  11. Hormone replacement therapy
  12. using mood stabilizer

Sites / Locations

  • CHINA

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Raloxifene

Placebo

Arm Description

Raloxifene Hydrochloride

placebo tablet

Outcomes

Primary Outcome Measures

Response in negative symptoms
A response in negative symptoms was defined as improvement of ≥20% compared with baseline PANSS negative score (12 weeks)

Secondary Outcome Measures

Clinical Assessment Interview for Negative Symptoms(CAINS)
The CAINS is a scale of the clinical assessment interview for negative symptoms of schizophrenia.The CAINS includes 16 items covering motivation and pleasure across social (five items), vocational (three items), and recreational life (three items) domains, as well as emotion expression and speech (five items).All items were rated on a scale of 0-4, with higher scores reflecting greater impairment.
Scale for the Assessment of Negative Symptoms (SANS)
The SANS are the most widely used symptom rating scales in schizophrenia research. SANS Total (Composite) score = sum(of SANS items 1-7, 9-12, 14-16, 18-21, and 23-24).The total range is from 0-120 scores.
Repeatable Battery for the Assessment of Neuropsychological Status(RBANS)
The RBANS is a brief cognitive screening battery consisting of 12 subtests which are used to create Index scores in the following five cognitive domains: Immediate Memory, Visuospatial/Constructional Skills, Language, Attention, and Delayed Memory. A total score is created by summing the five index cores which are thought to represent one's current neuropsychological status.
Hormone level change
Hormone level change over study duration (12 weeks)

Full Information

First Posted
January 22, 2018
Last Updated
September 4, 2019
Sponsor
Shanghai Mental Health Center
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1. Study Identification

Unique Protocol Identification Number
NCT03418831
Brief Title
Adjunctive Selective Estrogen Receptor Modulators on Negative and Cognitive Symptoms of Schizophrenia in Women
Official Title
Selective Estrogen Receptor Modulators - Adjunctive Treatment for Negative and Cognitive Symptoms of Schizophrenia in Postmenopausal Women
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
July 17, 2018 (Actual)
Primary Completion Date
April 30, 2019 (Actual)
Study Completion Date
July 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Mental Health Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the project is to assess the efficacy of Adjunctive Selective Estrogen Receptor Modulators (Raloxifene) on Negative and Cognitive symptoms of Schizophrenia in Postmenopausal Women. For postmenopausal women with schizophrenia, current research suggests that these people can be treated with estrogen, which can reduce cardiovascular and reproductive tissue problems, help sleep and improve mood. In addition, cognitive problems in this group of people can also be helped. Raloxifene is a Selective Estrogen Receptor Modulator (SERM), which means that it can affect the central nervous system (CNS) effects of estrogen (eg. improving emotional symptoms, memory, information processing and concentration), without adversely affecting reproductive tissue/organs such as breast, uterus and ovaries. The investigators are conducting a double-blind, placebo controlled, 12 weeks study comparing the negative symptoms and cognitive functions in postmenopausal women with schizophrenia in both groups. One group will receive clozapine plus 60mg Raloxifene (Usage: take 60mg Raloxifene tablets half an hour after breakfast every day, that is, take 1 tablet a day), while the second group will receive clozapine plus oral placebo (Usage: take 1 placebo half an hour after breakfast every day). Hypothesis 1: Adjuvant raloxifene therapy in postmenopausal women with schizophrenia can improve negative symptoms, as measured on the rating scales, compared with the women receiving adjunctive placebo. Hypothesis 2: The cognitive function of postmenopausal female schizophrenic patients treated with raloxifene would be better than that of the placebo group. Hypothesis 3: That the Raloxifene group has less adverse reactions in postmenopausal women with schizophrenia.
Detailed Description
Schizophrenia is a mental illness with unknown cause and difficult treatment which the global lifetime prevalence rate of about 1%. The core symptoms of schizophrenia include positive symptoms, negative symptoms, and impairment of cognitive function. Positive symptoms in most patients after antipsychotic treatment can significantly alleviate after antipsychotic treatment, but negative symptoms and cognitive deficits persist. Unfortunately, the long-term prognosis and social function of patients mainly depend on the degree of the rehabilitation of negative symptoms and cognitive function. At present, clinical research domestic and overseas on the negative symptoms and cognitive function gradually increased, but end up with the poor consistency of research results. The reason is various, but in any case, improving the treatment strategy is still very important. Epidemiological data suggest that the age of onset of female schizophrenia is later than men, most of which are onset abruptly, and females have higher susceptibility to mental illness and relapse during the two important periods with hormonal changes. The first is in the postpartum, menopause is the second. It may be related to the lack of estrogen function. Therefore, we believe that the onset and symptoms of some female patients with schizophrenia are related to the dysfunction of estrogen. Many studies abroad have found that estrogen and selective estrogen receptor modulators have significant effects on female patients with schizophrenia, especially on negative symptoms and cognitive functions, but the clinical application is limited due to the potential side effects of estrogen. Raloxifene is the second generation of selective estrogen receptor modulator, for the prevention and treatment of osteoporosis in postmenopausal women, which can significantly reduce the incidence of vertebral fractures. The common adverse drug reaction is slight increase in hot flash and leg cramps, and the most serious adverse drug reaction is venous thromboembolism. Past research has found that raloxifene can reduce the risk of decline in memory and attention, and taking raloxifene helps sleep. Current research suggests that as an adjuvant therapy, it can improve symptoms of menopausal women with schizophrenia (emotional symptoms, memory, information processing and storage), and will not negatively affect reproductive tissues or organs, such as breast, uterus and ovary. According to the domestic and overseas research results, and based on the theoretical background of schizophrenia in estrogen insufficiency, we proposed randomized double-blind placebo-controlled study, in order to understand the effect of raloxifene on negative symptoms and cognitive function in adjuvant treatment of menopausal female patients with schizophrenia, meanwhile assess the adverse reactions after the treatment, provide the basis for clinical treatment of schizophrenia patients with negative symptoms and cognitive impairment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
negtive symptoms, cognitive function

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Raloxifene
Arm Type
Active Comparator
Arm Description
Raloxifene Hydrochloride
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo tablet
Intervention Type
Drug
Intervention Name(s)
Raloxifene Hydrochloride
Other Intervention Name(s)
Evista
Intervention Description
60 mg per capsule (1 tablet daily) for 12 weeks
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
Starch capsule
Intervention Description
1 tablet daily for 12 weeks
Primary Outcome Measure Information:
Title
Response in negative symptoms
Description
A response in negative symptoms was defined as improvement of ≥20% compared with baseline PANSS negative score (12 weeks)
Time Frame
baseline, week 4, 8, 12
Secondary Outcome Measure Information:
Title
Clinical Assessment Interview for Negative Symptoms(CAINS)
Description
The CAINS is a scale of the clinical assessment interview for negative symptoms of schizophrenia.The CAINS includes 16 items covering motivation and pleasure across social (five items), vocational (three items), and recreational life (three items) domains, as well as emotion expression and speech (five items).All items were rated on a scale of 0-4, with higher scores reflecting greater impairment.
Time Frame
baseline, week 4, 8, 12
Title
Scale for the Assessment of Negative Symptoms (SANS)
Description
The SANS are the most widely used symptom rating scales in schizophrenia research. SANS Total (Composite) score = sum(of SANS items 1-7, 9-12, 14-16, 18-21, and 23-24).The total range is from 0-120 scores.
Time Frame
baseline, week 4, 8, 12
Title
Repeatable Battery for the Assessment of Neuropsychological Status(RBANS)
Description
The RBANS is a brief cognitive screening battery consisting of 12 subtests which are used to create Index scores in the following five cognitive domains: Immediate Memory, Visuospatial/Constructional Skills, Language, Attention, and Delayed Memory. A total score is created by summing the five index cores which are thought to represent one's current neuropsychological status.
Time Frame
baseline, week 12
Title
Hormone level change
Description
Hormone level change over study duration (12 weeks)
Time Frame
baseline, week 4, 8, 12

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Outpatient or inpatient, aged more than 45 years, postmenopausal female (menopause for more than one year) International Classification of Diseases, Tenth Revision, diagnosis of schizophrenia Continue to receive antipsychotic clozapine for more than 2 years with a stable dose of at least one month Negative symptoms scale >20 in PANSS, and a score of 4 (moderate) or more on one or more of N1-N7, and within two weeks before intervention, the total score of negative symptom factors improved by no more than 10% Able to give informed consent Exclusion Criteria: Participating in other clinical studies Previous use of raloxifene intolerable Hormone related endocrine disease Acute liver disease thrombotic disease Estrogen dependent tumor Hyperthyreosis Severe cardiac dysfunction or renal disease Diabetes mellitus Abnormal uterine bleeding or cerebrovascular accident Hormone replacement therapy using mood stabilizer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
LV QINYU
Organizational Affiliation
SHANGHAI MENTAL HEALTH CENTRE
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHINA
City
Shanghai
State/Province
Minhang
ZIP/Postal Code
201108
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Adjunctive Selective Estrogen Receptor Modulators on Negative and Cognitive Symptoms of Schizophrenia in Women

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