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Treatment of Schizoaffective Disorder Using Mifepristone

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Stanford University

Status and phase

Terminated
Phase 3
Phase 2

Conditions

Psychotic Disorders
Depressive Disorder, Major
Depressive Disorder

Treatments

Drug: Placebo Oral Tablet
Drug: Mifepristone

Study type

Interventional

Funder types

Other

Identifiers

NCT00725270
76458
SU-06012008-1191

Details and patient eligibility

About

This study tests the hypothesis that mifepristone will diminish cognitive distortion and alleviate psychosis in patients with schizoaffective disorder.

Full description

You are invited to participate in a research study which evaluates the effectiveness of mifepristone (RU 486) in rapidly reducing the symptoms associated with schizoaffective disorder. Our group believes that the cognitive deficits (a decline in the ability to think clearly) and psychosis (hallucinations or delusions) exhibited in some affective disorders are driven by an excess of stress hormone effects (hypercortisolemia). Often the origin of this hormonal imbalance is unknown. Current treatment for schizoaffective disorder (characterized by mood swings and hallucinations and/or delusions) involves using a combination of antidepressant medication (for mood elevation), mood stabilizing medications (to prevent extreme high and low moods) and antipsychotic medication (for the correction of altered thinking). While these therapies are often effective, they can take several weeks or longer to work. We hope to uncover a quick, effective, safe therapy for the treatment of individuals with your condition.

Enrollment

12 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:The subjects will be 30 inpatients or outpatients with schizoaffective disorder. Exclusion Criteria:Subjects must be between the ages of eighteen and seventy-five without major medical problems.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

12 participants in 2 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
Patients will be randomized to placebo
Treatment:
Drug: Placebo Oral Tablet
Mifepristone
Experimental group
Description:
Patients will be randomized to mifepristone
Treatment:
Drug: Mifepristone

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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