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Schizophrenia in Post Menopausal WomenPhase 3NCT01573637

Raloxifene as an Adjuvant Treatment of the Negative Symptoms of Schizophrenia in Post-menopausal Women

A Phase 3 study testing Raloxifene in people with Schizophrenia in Post Menopausal Women, run by Fundació Sant Joan de Déu at 3 sites in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The efficacy of raloxifene versus placebo was compared over a six-month period, as an adjuvant treatment of the negative symptoms of schizophrenia in a group of 80 post-menopausal women. Read more about this study

Who is it for?
Ages 45 years and older, women only
Conditions the study is for
Schizophrenia in Post Menopausal Women
What is being tested?
Raloxifene
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
78 participants
Where
3 sitesSpain
Study dates
Jul 2011to Jul 2014
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Diagnosis of schizophrenia according to DSM-IV TR criteria.
  • Postmenopausal patients. Post-menopausal is defined as 1) aged over 45 years with at least one year of amenorrhea and levels of FSH over 20 UI/L or 2) aged over 50 years with at least one year of amenorrhea.
  • Patients who have been taking a stable dose of antispsychotic medication for at least the 30 days before the start of the study.
  • The presence of significant negative symptoms (defined as one or more negative symptoms with a severity of over 4 on the PANSS scale).
  • General written informed consent by patients or their legal representative.
  • For the genotypic study, a specific informed consent signed by the patients or legal representative is required.

Who cannot join

  • A diagnosis of substance abuse/dependence in the previous 6 months.
  • Mental retardation
  • A diagnosis of major depression (according to DSM-IV TR criteria).
  • Endocrine alterations related to sexual hormones, liver insufficiency including cholestasis, severe renal insufficiency.
  • History or current condition of thromboembolism, breast cancer, abnormal uterine bleeding or stroke.
  • Patients in hormone replacement therapy.
Show all 9Show fewer
  • Known allergy or hypersensitivity to the active ingredient of the investigational drug, or to any of its excipients or lactose.
  • To be receiving treatment in another clinical trial.
  • To present any severe concomitant disease that in the researcher's opinion can compromise completion of the study or affect the patient's tolerance to this treatment.

Trial locations and contacts

3 sites in 1 country.

Spain3 sites
  • Hospital Psiquiàtric Institut Pere Mata

    Reus, Tarragona, 43206

  • Corporació Sanitària Parc Taulí

    Sabadell, Barcelona, 08208

  • Parc Sanitari Sant Joan de Déu

    Sant Boi de Llobregat, Barcelona, 08830

Other trials in Spain

About this study

Official title: Six Month, Double Blind, Placebo-controlled Trial of the Efficacy of Raloxifene as an Adjuvant Treatment of the Negative Symptoms of Schizophrenia in Post-menopausal Women

The efficacy of raloxifene versus placebo was compared over a six-month period, as an adjuvant treatment of the negative symptoms of schizophrenia in a group of 80 post-menopausal women. The aim of the study is to analyze whether raloxifene has an effect on the positive and negative symptoms of schizophrenia, and on psychopathological symptoms in general, and on social and neuropsychological functioning, and to study the influence of genetic polymorphisms in treatment response.

Read the detailed description

Several studies have found gender-related differences in the epidemiology, clinical presentation, clinical course and response to treatment of schizophrenic disorder(1,2). Findings relating to a lower frequency of schizophrenia in women, its later onset and less severe clinical course(3,4), have led to the appearance of the "estrogen hypothesis" of schizophrenia, which postulates that estrogen has a protective effect in women susceptible to this disease(5).

The estrogen hypothesis in relation to schizophrenia is based on several studies that showed that estrogen levels are significantly lower in schizophrenic women than in healthy women,(6) and that outbreaks or onset of the disease tend to coincide with stages of the menstrual cycle in which estrogen levels are the lowest(7,8).

Studies on experimental animals have shown that estrogen has a modulating effect on the brain dopaminergic system(9,10) and that it also affects serotoninergic activity(11). Estrogens also enhance neuronal regeneration and block mechanisms of neuronal death(12).

The discovery that estrogen has a modulatory effect on the dopaminergic system has encouraged some researchers to study the therapeutic use of estrogen in schizophrenic patients. Several double-blind clinical trials have shown that estrogens are effective at improving psychotic symptoms(13-15). These last studies analyzed the efficacy of estrogens after one and two months, and mainly in relation to positive symptoms, in patients with the acute illness. However, in older patients it is the severity of the negative, rather than the positive, symptoms that seems to be associated with a poorer cognitive and social function. Moreover, positive symptoms tend to be less severe with age, while negative symptoms tend to persist(16).

Regarding the possible use of estrogens to treat post-menopausal women with schizophrenia, Lindamer et al.,(17) studied the psychopathology of menopausal patients with schizophrenia and found that patients in hormone replacement therapy required lower doses of antipsychotic drugs and presented less negative symptoms, whereas no differences were found in response to treatment in relation to positive symptoms.

The greater frequency of later onset schizophrenia in women than in men seems to be related to the drop in estrogen levels that occurs during the menopause. Häfner et al.(19) found that schizophrenia of late onset was more severe in women than in men, especially in relation to negative symptoms, and these results also appear to support the hypothesis that estrogens act as a protective factor before the menopause.

The use of estrogens as adjuvant therapy in schizophrenia seems promising, although in long-term treatment it can have a potentially negative effect on breast and uterine tissue(20,21). This was the reason we chose raloxifene for our study, which is a selective estrogen receptor modulator (SERM) that can act as a tissue-selective agonist or antagonist. Raloxifene is a first-generation SERM used in the preventive treatment of post-menopausal osteoporosis and does not affect breast or ovarian tissue. (22). It has agonistic effects on the brain(23). Raloxifene seems to influence multiple neurotransmission pathways, including that of seratonin in the frontal cortex, basal and striated ganglia(24), areas of the brain that are commonly affected in schizophrenic patients.

There is some evidence that raloxifene can be useful in the treatment of some mental disorders in post-menopausal women(25,26). Recently, Kulkarni et al.(27) have reported preliminary data that also seem to support a role for raloxifene in schizophrenic patients.

Our team conducted a 12-week, randomized, double-blind, placebo-controlled clinical trial funded by the Stanley Foundation, to assess the value of 60 mg of raloxifene as adjuvant treatment for the negative symptoms, and other psychotic symptoms, in post-menopausal women. In our study on 33 patients, we found that women in the raloxifene group showed a greater improvement in both positive and negative symptoms, and also in general psychopathological symptoms, than women who had only received antipsychotic medication(28).

Since part of Raloxifene's mechanism of action involves activating the estrogenic receptors, some studies have explored the possibility that polymorphisms in these alfa (ESR1) or beta (ESR2) estrogenic receptor genes can modify the effects of treatment with raloxifene(29-31). Several pharmacogenomic studies have reported that single nucleotide polymorphisms (SNPs) in these genes, affect raloxifene treatment in relation to its endothelial function(29), cholesterol levels(30) and bone mineral density(31). Nevertheless, no studies have assessed whether these SNPs of ESR1 or ESR2 can influence raloxifene's effects in the brain. Based on the positive results of our preliminary study, we have designed a longer clinical trial with the same dose of raloxifene that had been effective in the first study. We aim to include in this 6-month placebo-controlled, randomized, double-blind clinical trial a larger number of post-menopausal women with schizophrenia, and improve the clinical assessments by using a larger battery of psychometric tests in areas of social functioning and neuropsychological performance. Genotypic studies will be conducted of the 4 SNPs in the ESR1 (rs9340799, rs2234693, rs1801132) and ESR2 (rs1256049) genes, to control the effects of patients' genotypes on response to treatment.

DESCRIPTION OF THE TARGET POPULATION

The sample includes post-menopausal women diagnosed with schizophrenia according to DSM-IV-TR criteria.

Post-menopause is defined as 1) aged over 45 years with a minimum of one year of amenorrhea and FSH levels higher than 20 UI/L or 2) aged over 50 years old with at least one year of amenorrhea.

Being tested
Raloxifene, Lactosa (placebo arm)
Keywords
schizophrenia, negative schizophrenia, schizophrenia in post-menopausal women, schizophrenia in women, ralixifene, raloxifen, raloxifeno, negative symptoms of schizophrenia, negative symptoms in schizophrenia, schizophrenia symptoms, negative symptoms of psychosis
Medical subject headings
Schizophrenia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • RaloxifeneDrug

    Also called Raloxifene hydrochloride 60 mg, Laboratory Esteve.

    The dose of raloxifene hydrochloride administered will be 60 mg/day. Both placebo and the raloxifene will be administered over 6 months. Patients will take one single daily dose administered in the morning. Drug will be given orally in capsule form.

  • Lactosa (placebo arm)Drug

    Also called Lactosa

    Both placebo and the raloxifene will be administered over 6 months. Patients will take one single daily dose administered in the morning. Drug will be given orally in capsule form.

Study groups in NCT01573637
Study groupRoleWhat they receive
Raloxifene hydrochloride 60 mgExperimentalPatients fulfilling inclusion criteria and those giving the general informed consent for the study will be randomly allocated to one of the two groups in the trial (placebo or raloxifene) in a 1:1 proportion and in blocks of 4 patients, using the random number tables designed for this purpose. The dose of raloxifene hydrochloride administered will be 60 mg/day. Both placebo and the raloxifene will be administered over 6 months. Patients will take one single daily dose administered in the morning. Both drugs will be given orally in capsule form. The medication of each of the treatment groups (lactose as placebo, raloxifene) will be introduced into dark green gelatin capsules to guarantee the blinding.
Receives: Drug: Raloxifene
Lactosa (placebo)Placebo comparatorPatients fulfilling inclusion criteria and those giving the general informed consent for the study will be randomly allocated to one of the two groups in the trial (placebo or raloxifene) in a 1:1 proportion and in blocks of 4 patients, using the random number tables designed for this purpose. The dose of raloxifene hydrochloride administered will be 60 mg/day. Both placebo and the raloxifene will be administered over 6 months. Patients will take one single daily dose administered in the morning. Both drugs will be given orally in capsule form. The medication of each of the treatment groups (lactose as placebo, raloxifene) will be introduced into dark green gelatin capsules to guarantee the blinding.
Receives: Drug: Lactosa (placebo arm)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To assess the efficacy of raloxifene (SERM - Selective Estrogen Receptor Modulator) as an adjuvant of antipsychotic treatment in the management of negative symptoms of schizophrenia in post-menopausal women.

    The primary variable of efficacy will correspond to the change in score on the negative subscale of the PANSS from the start of treatment to the final assessment at 24 weeks. Patients will be considered to respond to treatment if the score in the negative subscale is at least 20% lower than at the start of treatment.

    Measured: Change in score on the negative subscale of the PANSS from baseline to final assessment at week 24

Secondary outcomes (5)
  1. To assess the efficacy of raloxifene as an adjuvant of antipsychotic treatment in the management of global symptoms of schizophrenia in postmenopausal women.

    The results from different scales or test will be measured: at baseline,week 4,12 y 24 for scales (PANSS, SANS, CGI, GAF, CDSS -Calgary, LSP, SIMPSON, UKU, DAS-sv) and at baseline, week 12 and 24 for neuropsychological test (TAVEC, CPT, TMT, STROOP, FAS, WAIS sub-tests).

    Measured: From baseline to week 24 (measurements at Baseline, weeks 4, 12, 24)

  2. To assess the efficacy of raloxifene as an adjuvant of antipsychotic treatment in the global functioning of postmenopausal women with schizophrenia.

    The results from different scales or test will be measured: at baseline,week 4,12 y 24 for scales (PANSS, SANS, CGI, GAF, CDSS -Calgary, LSP, SIMPSON, UKU, DAS-sv) and at baseline, week 12 and 24 for neuropsychological test (TAVEC, CPT, TMT, STROOP, FAS, WAIS sub-tests).

    Measured: From baseline to week 24 (measurements at Baseline, weeks 4, 12, 24)

  3. To assess the efficacy of raloxifene as an adjuvant of antipsychotic treatment in the neuropsychological functioning of post-menopausal women with schizophrenia

    The results from different test will be measured at weeks, baseline, 12 and 24 for neuropsychological test (TAVEC, CPT, TMT, STROOP, FAS, WAIS sub-tests).

    Measured: From baseline to week 24 (measurements at Baseline, week 12, week 24)

  4. To control response to treatment as a function of genetic variants in the form of SNP (Single Nucleotide Polymorphisms) that patients present in the alfa (ESR1) and beta (ESR2) estrogenic receptor genes.

    Analysis will be done for patients who consented by the Informed Consent Form. The analysis will be carried out by centralized laboratory (Biobanc Institut d´Investigació Sanitària Pere Virgili; Reus, Spain) once all samples will be collected. In the meantime, the samples will be kept frozen at 4oC.

    Measured: Blood sample collected at Baseline visit

  5. To assess the safety of the medication used in this patient population.

    Safety will be assessed during the study by the vigilance of the AEs, SAEs, AR, SARs at each visit. Blood analysis (hemo/chem) will be done at Baseline and at the end (week 24), and clinical scales will be measured at Baseline, week 4,12 y 24 (PANSS, SANS, CGI, GAF, CDSS -Calgary, LSP, SIMPSON, UKU, DAS-sv)

    Measured: From Baseline to week 24

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Apr 2012 (estimated)
  2. Study startJul 2011
  3. Primary completionJul 2014
  4. Study completionJul 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
78 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01573637
Sponsor's protocol ID
FSJD-RAL-2010
Status last verified
Apr 2024
First submitted
5 Apr 2012
Last updated
22 Apr 2024
Results posted
No
Data monitoring committee
No

Publications

  • Leung A, Chue P. Sex differences in schizophrenia, a review of the literature. Acta Psychiatr Scand Suppl. 2000;401:3-38. doi: 10.1111/j.0065-1591.2000.0ap25.x.

    PubMed 10887978
  • Hafner H. Gender differences in schizophrenia. Psychoneuroendocrinology. 2003 Apr;28 Suppl 2:17-54. doi: 10.1016/s0306-4530(02)00125-7.

    PubMed 12650680
  • Jablensky A, Sartorius N, Ernberg G, Anker M, Korten A, Cooper JE, Day R, Bertelsen A. Schizophrenia: manifestations, incidence and course in different cultures. A World Health Organization ten-country study. Psychol Med Monogr Suppl. 1992;20:1-97. doi: 10.1017/s0264180100000904. No abstract available.

    PubMed 1565705
  • Usall J, Busquets E, Araya S, Ochoa S, Gost A. [Gender differences in schizophrenia. A literature review]. Actas Esp Psiquiatr. 2000 May-Jun;28(3):178-85. Spanish.

    PubMed 11000700
  • Seeman MV, Lang M. The role of estrogens in schizophrenia gender differences. Schizophr Bull. 1990;16(2):185-94. doi: 10.1093/schbul/16.2.185.

    PubMed 2197713
  • Riecher-Rossler A, Hafner H, Stumbaum M, Maurer K, Schmidt R. Can estradiol modulate schizophrenic symptomatology? Schizophr Bull. 1994;20(1):203-14. doi: 10.1093/schbul/20.1.203.

    PubMed 8197416
  • Riecher-Rössler A, Häfner H, Maurer K, Stummbaum M, Schmitd R. Schizophrenia symptomatology varies with serum estradiol levels during menstrual cycle. Schizophrenia Research 1992; 6: 114-115.

  • Huber TJ, Rollnik J, Wilhelms J, von zur Muhlen A, Emrich HM, Schneider U. Estradiol levels in psychotic disorders. Psychoneuroendocrinology. 2001 Jan;26(1):27-35. doi: 10.1016/s0306-4530(00)00034-2.

    PubMed 11070332
  • Di Paolo T, Bedard F, Bedard PJ. Influence of gonadal steroids on human and monkey cerebrospinal fluid homovanillic acid concentrations. Clin Neuropharmacol. 1989 Feb;12(1):60-6. doi: 10.1097/00002826-198902000-00008.

    PubMed 2469538
  • Hafner H, Behrens S, De Vry J, Gattaz WF. An animal model for the effects of estradiol on dopamine-mediated behavior: implications for sex differences in schizophrenia. Psychiatry Res. 1991 Aug;38(2):125-34. doi: 10.1016/0165-1781(91)90038-q.

    PubMed 1754627
  • Moses EL, Drevets WC, Smith G, Mathis CA, Kalro BN, Butters MA, Leondires MP, Greer PJ, Lopresti B, Loucks TL, Berga SL. Effects of estradiol and progesterone administration on human serotonin 2A receptor binding: a PET study. Biol Psychiatry. 2000 Oct 15;48(8):854-60. doi: 10.1016/s0006-3223(00)00967-7.

    PubMed 11063980
  • DonCarlos LL, Azcoitia I, Garcia-Segura LM. Neuroprotective actions of selective estrogen receptor modulators. Psychoneuroendocrinology. 2009 Dec;34 Suppl 1:S113-22. doi: 10.1016/j.psyneuen.2009.04.012.

    PubMed 19447561
  • Kulkarni J, Riedel A, de Castella AR, Fitzgerald PB, Rolfe TJ, Taffe J, Burger H. Estrogen - a potential treatment for schizophrenia. Schizophr Res. 2001 Mar 1;48(1):137-44. doi: 10.1016/s0920-9964(00)00088-8.

    PubMed 11278160
  • Akhondzadeh S, Nejatisafa AA, Amini H, Mohammadi MR, Larijani B, Kashani L, Raisi F, Kamalipour A. Adjunctive estrogen treatment in women with chronic schizophrenia: a double-blind, randomized, and placebo-controlled trial. Prog Neuropsychopharmacol Biol Psychiatry. 2003 Sep;27(6):1007-12. doi: 10.1016/S0278-5846(03)00161-1.

    PubMed 14499318
  • Kulkarni J, de Castella A, Fitzgerald PB, Gurvich CT, Bailey M, Bartholomeusz C, Burger H. Estrogen in severe mental illness: a potential new treatment approach. Arch Gen Psychiatry. 2008 Aug;65(8):955-60. doi: 10.1001/archpsyc.65.8.955.

    PubMed 18678800

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Raloxifene in people with Schizophrenia in Post Menopausal Women, run by Fundació Sant Joan de Déu at 3 sites in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To assess the efficacy of raloxifene (SERM - Selective Estrogen Receptor Modulator) as an adjuvant of antipsychotic treatment in the management of negative symptoms of schizophrenia in post-menopausal women. (time frame: Change in score on the negative subscale of the PANSS from baseline to final assessment at week 24). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01573637, which also lists 33 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Apr 2024.

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