Estradiol Patch as add-on to Antipsychotics in Patients With Schizophrenia, Schizoaffective or Schizophreniform Disorder

Schizophrenia Clinical Trial

Official title:

A Randomized Trial Administering Estradiol Patch vs. Placebo Patch as add-on to Antipsychotics in Patients With Schizophrenia, Schizoaffective or Schizophreniform Disorder

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03848234
• Other study ID #: EST-S-01
• Status: Completed
• Phase: Phase 3
• Start date: December 4, 2015
• Est. completion date: July 29, 2016

Study information

• Verified date: February 2019
• Source: Tangent Data
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate the effects of Estradiol patches vs placebo patches as add-on to antipsychotics on psychometric performance in patients with schizophrenia, schizoaffective or schizophreniform disorder

Description:

Estradiol has been shown to be an effective adjunctive treatment for schizophrenia. The estradiol hypothesis was tested in a randomized-controlled trial in which estradiol was given to women with schizophrenia, schizoaffective or schizophreniform disorder aged 18 to 45 - Kulkarni 2014. In that 3 arms trial, Kulkarni administered transdermal 100 µg estradiol/200 µg estradiol/ placebo to patients receiving anti-psychotics and reported reductions in PANSS positive, general and total symptoms in both estradiol patients' groups compared with the placebo group. Patients receiving 200 µg experienced greater improvement, specifically in the PANSS positive subscale, the effect size was 0.44.

The objective of this study is to attempt to confirm Kulkarni's trial in a large-scale trial. This proposed study is a 2-arm study, in which patients will be randomized to either 200 µg estradiol or placebo in order to test the effectiveness of estradiol on women of childbearing age with schizophrenia, schizoaffective or schizophreniform disorder for a limited period of 56 days.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 209
• Est. completion date: July 29, 2016
• Est. primary completion date: July 29, 2016
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Female, 18-45 years of age, inclusive

2. Willing and able to provide informed consent, after the nature of the study has been fully explained

3. Current DSM-IV-TR diagnosis of schizophrenia, schizoaffective or schizophreniform disorder as confirmed by modified SCID.

4. Total PANSS score > 60 and (PANSS positive subscale >15 and/or PANSS negative subscale >15)

5. Must be on a stable dose of any antipsychotic drug, for at least 2 weeks prior to the baseline visit, at doses within the PORT criteria, whenever possible. Patients receiving higher doses will have their records reviewed to insure that their dose is required and, if possible, will be stabilized on a lower dose prior to study entry.

6. Patients who are physically and endocrinologically healthy,

7. Inpatients or outpatients. Inpatients will be randomized 3 days or more after admission

Exclusion Criteria:

1. Unwilling or unable, in the opinion of the Investigator, to comply with study instructions

2. Pregnant or breast-feeding

3. Women who are menopausal.

4. Patients treated with oral estrogen preparations containing estradiol greater than 30 mcg.

5. Women who have known severe abnormalities in the hypothalamo-pituitary gonadal axis, thyroid disorders, severe medical conditions and disorders that would contraindicate estrogen use (breast cancer, migraine with aura or stroke)

6. History of endometrial cancer or breast cancer, vaginal bleeding between periods, untreated endometrial hyperplasia, previous or present thrombembolism, known thrombophilic disorders, abnormal liver function tests, porphyria.

7. History of 1st and 2nd grade family with breast or uterine cancer,

8. Likely allergy or sensitivity to estradiol.

9. Schizoaffective disorder in the manic phase.

10. At significant risk of committing suicide, or in the opinion of the Investigator, currently is at imminent risk of suicide or harming others.

11. Patients with a current DSM-IV substance or alcohol abuse. Patients with a history of and/or current recreational use of cannabinoids or alcohol, and/or patients who smoke cigarettes can be included.

12. Concurrent delirium, mental retardation, drug-induced psychosis, or history of clinically significant brain trauma documented by CT or MRI.

13. Patients receiving phenobarbital, phenytoin, carbamazepine, rifampicin, rifabutin, nevirapine, efavirenz, ritonavir and nelfinavir,or Hypericum perforatum

Related Conditions & MeSH terms

• Disease
• Psychotic Disorders
• Schizoaffective Disorder
• Schizophrenia
• Schizophreniform Disorders

Intervention

Drug:
• Estradiol
2 trans dermal patches to be changed twice a week for the duration of 8 weeks.

Device:
• Placebo
2 trans dermal patches to be changed twice a week for the duration of 8 weeks.

Locations

Country	Name	City	State
Moldova, Republic of	Clinical Psychiatric Hospital	Codru	Chisinau

Sponsors (2)

Lead Sponsor	Collaborator
Tangent Data	Stanley Medical Research Institute

Country where clinical trial is conducted

Moldova, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PANSS positive subscale at the end of the trial	To evaluate the effects of Estradiol on Positive and Negative Syndrome Scale for Schizophrenia (PANSS)	8 weeks
Secondary	PANSS total, negative and general psychopathology scales	To evaluate the effects of Estradiol on Positive and Negative Syndrome Scale for Schizophrenia (PANSS)	8 weeks
Secondary	Clinical Global Impression Scale-Severity (CGI-S) and Global Impression Scale-Improvement (CGI-I)	To evaluate the effects of Estradiol on Clinical Global Impression	8 weeks
Secondary	Brief Assessment of Cognition in Schizophrenia (BACS),	To evaluate the effects of Estradiol on cognition	8 weeks
Secondary	Montgomery-Asberg Depression Rating Scale	To evaluate the effects of Estradiol on depressive symptoms	8 weeks
Secondary	Rates of drop outs before the end of the trial	To evaluate the rate of drop outs	through study completion, an average of 1 year