Estradiol Patch as add-on to Antipsychotics in Patients With Schizophrenia, Schizoaffective or Schizophreniform Disorder
Primary Purpose
Schizophrenia, Schizoaffective Disorder, Schizophreniform Disorders
Status
Completed
Phase
Phase 3
Locations
Moldova, Republic of
Study Type
Interventional
Intervention
Estradiol
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Schizophrenia
Eligibility Criteria
Inclusion Criteria:
- Female, 18-45 years of age, inclusive
- Willing and able to provide informed consent, after the nature of the study has been fully explained
- Current DSM-IV-TR diagnosis of schizophrenia, schizoaffective or schizophreniform disorder as confirmed by modified SCID.
- Total PANSS score > 60 and (PANSS positive subscale >15 and/or PANSS negative subscale >15)
- 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.
- Patients who are physically and endocrinologically healthy,
- Inpatients or outpatients. Inpatients will be randomized 3 days or more after admission
Exclusion Criteria:
- Unwilling or unable, in the opinion of the Investigator, to comply with study instructions
- Pregnant or breast-feeding
- Women who are menopausal.
- Patients treated with oral estrogen preparations containing estradiol greater than 30 mcg.
- 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)
- 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.
- History of 1st and 2nd grade family with breast or uterine cancer,
- Likely allergy or sensitivity to estradiol.
- Schizoaffective disorder in the manic phase.
- At significant risk of committing suicide, or in the opinion of the Investigator, currently is at imminent risk of suicide or harming others.
- 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.
- Concurrent delirium, mental retardation, drug-induced psychosis, or history of clinically significant brain trauma documented by CT or MRI.
- Patients receiving phenobarbital, phenytoin, carbamazepine, rifampicin, rifabutin, nevirapine, efavirenz, ritonavir and nelfinavir,or Hypericum perforatum
Sites / Locations
- Clinical Psychiatric Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
A Estradiol
B Placebo
Arm Description
2 trans dermal patches to be changed twice a week for the duration of 8 weeks
2 trans dermal patches to be changed twice a week for the duration of 8 weeks
Outcomes
Primary Outcome Measures
PANSS positive subscale at the end of the trial
To evaluate the effects of Estradiol on Positive and Negative Syndrome Scale for Schizophrenia (PANSS)
Secondary Outcome Measures
PANSS total, negative and general psychopathology scales
To evaluate the effects of Estradiol on Positive and Negative Syndrome Scale for Schizophrenia (PANSS)
Clinical Global Impression Scale-Severity (CGI-S) and Global Impression Scale-Improvement (CGI-I)
To evaluate the effects of Estradiol on Clinical Global Impression
Brief Assessment of Cognition in Schizophrenia (BACS),
To evaluate the effects of Estradiol on cognition
Montgomery-Asberg Depression Rating Scale
To evaluate the effects of Estradiol on depressive symptoms
Rates of drop outs before the end of the trial
To evaluate the rate of drop outs
Full Information
NCT ID
NCT03848234
First Posted
February 13, 2019
Last Updated
May 20, 2020
Sponsor
Tangent Data
Collaborators
Stanley Medical Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT03848234
Brief Title
Estradiol Patch as add-on to Antipsychotics in Patients With Schizophrenia, Schizoaffective or Schizophreniform Disorder
Official Title
A Randomized Trial Administering Estradiol Patch vs. Placebo Patch as add-on to Antipsychotics in Patients With Schizophrenia, Schizoaffective or Schizophreniform Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
December 4, 2015 (Actual)
Primary Completion Date
July 29, 2016 (Actual)
Study Completion Date
July 29, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tangent Data
Collaborators
Stanley Medical Research Institute
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
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
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder, Schizophreniform Disorders
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Randomized, add-on to anti-psychotics, double blind, placebo-controlled, parallel group clinical trial
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
209 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A Estradiol
Arm Type
Experimental
Arm Description
2 trans dermal patches to be changed twice a week for the duration of 8 weeks
Arm Title
B Placebo
Arm Type
Placebo Comparator
Arm Description
2 trans dermal patches to be changed twice a week for the duration of 8 weeks
Intervention Type
Drug
Intervention Name(s)
Estradiol
Other Intervention Name(s)
trans dermal patches
Intervention Description
2 trans dermal patches to be changed twice a week for the duration of 8 weeks.
Intervention Type
Device
Intervention Name(s)
Placebo
Other Intervention Name(s)
trans dermal patches
Intervention Description
2 trans dermal patches to be changed twice a week for the duration of 8 weeks.
Primary Outcome Measure Information:
Title
PANSS positive subscale at the end of the trial
Description
To evaluate the effects of Estradiol on Positive and Negative Syndrome Scale for Schizophrenia (PANSS)
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
PANSS total, negative and general psychopathology scales
Description
To evaluate the effects of Estradiol on Positive and Negative Syndrome Scale for Schizophrenia (PANSS)
Time Frame
8 weeks
Title
Clinical Global Impression Scale-Severity (CGI-S) and Global Impression Scale-Improvement (CGI-I)
Description
To evaluate the effects of Estradiol on Clinical Global Impression
Time Frame
8 weeks
Title
Brief Assessment of Cognition in Schizophrenia (BACS),
Description
To evaluate the effects of Estradiol on cognition
Time Frame
8 weeks
Title
Montgomery-Asberg Depression Rating Scale
Description
To evaluate the effects of Estradiol on depressive symptoms
Time Frame
8 weeks
Title
Rates of drop outs before the end of the trial
Description
To evaluate the rate of drop outs
Time Frame
through study completion, an average of 1 year
10. Eligibility
Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Female, 18-45 years of age, inclusive
Willing and able to provide informed consent, after the nature of the study has been fully explained
Current DSM-IV-TR diagnosis of schizophrenia, schizoaffective or schizophreniform disorder as confirmed by modified SCID.
Total PANSS score > 60 and (PANSS positive subscale >15 and/or PANSS negative subscale >15)
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.
Patients who are physically and endocrinologically healthy,
Inpatients or outpatients. Inpatients will be randomized 3 days or more after admission
Exclusion Criteria:
Unwilling or unable, in the opinion of the Investigator, to comply with study instructions
Pregnant or breast-feeding
Women who are menopausal.
Patients treated with oral estrogen preparations containing estradiol greater than 30 mcg.
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)
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.
History of 1st and 2nd grade family with breast or uterine cancer,
Likely allergy or sensitivity to estradiol.
Schizoaffective disorder in the manic phase.
At significant risk of committing suicide, or in the opinion of the Investigator, currently is at imminent risk of suicide or harming others.
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.
Concurrent delirium, mental retardation, drug-induced psychosis, or history of clinically significant brain trauma documented by CT or MRI.
Patients receiving phenobarbital, phenytoin, carbamazepine, rifampicin, rifabutin, nevirapine, efavirenz, ritonavir and nelfinavir,or Hypericum perforatum
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paull G Radu, M.D.
Organizational Affiliation
Tangent Data
Official's Role
Study Director
Facility Information:
Facility Name
Clinical Psychiatric Hospital
City
Codru
State/Province
Chisinau
ZIP/Postal Code
2011
Country
Moldova, Republic of
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
31365044
Citation
Weiser M, Levi L, Zamora D, Biegon A, SanGiovanni JP, Davidson M, Burshtein S, Gonen I, Radu P, Slobozean Pavalache K, Nastas I, Hemi R, Ryan T, Davis JM. Effect of Adjunctive Estradiol on Schizophrenia Among Women of Childbearing Age: A Randomized Clinical Trial. JAMA Psychiatry. 2019 Oct 1;76(10):1009-1017. doi: 10.1001/jamapsychiatry.2019.1842.
Results Reference
derived
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Estradiol Patch as add-on to Antipsychotics in Patients With Schizophrenia, Schizoaffective or Schizophreniform Disorder
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