Trial Search Results
Mifepristone Treatment for Patients With Non-psychotic Major Depressive Disorder Receiving Bilateral ECT
The purpose of this study is to see whether the medication mifepristone is an effective and tolerable treatment for increasing the clinical effectiveness of electroconvulsive therapy (ECT) and protecting cognitive function during ECT. Both Mifepristone and ECT appear to normalize hyperfunctioning of the hypothalmic-pituitary-adrenal (HPA) axis, which has been found among patients with major depression referred for ECT. The combination of these two treatments in major depression may lead to a more rapid clinical response than ECT alone. Additionally, there appears to be a connection between pre-ECT higher cortisol levels due to HPA axis hyperfunctioning and post-ECT cognitive impairment. Administration of mifepristone prior to and during ECT treatment may reduce cortisol levels and reduce the incidence of cognitive impairment observed after ECT.
Stanford is currently not accepting patients for this trial.
- Drug: Mifepristone
- Drug: Placebo Oral Capsule
Inclusion Criteria:To be considered for participation in the study, subject must meet all
of the following criteria:
1. Meets DSM-IV criteria for Major Depressive Episode without psychotic features.
2. 18-75 years of age and able to provide legal consent.
3. Referred to Stanford ECT service by treating physician for bilateral electroconvulsive
therapy with inpatient hospitalization.
4. Completed process for consenting to the clinical use of ECT according to California
5. Females of childbearing potential must be using a double-barrier method of
contraception during the study and for 30 days after the study (modified 6-2003)
Exclusion Criteria:Subjects will be excluded from participation if they meet any of the
1. Treatment with ECT in the 6 months prior to screening.
2. Meets criteria for drug or alcohol abuse or dependence in the 6 months prior to
3. Use of alcohol or illegal drugs within seven days of randomization or during study.
4. Presence of unstable or untreated cardiovascular disease, hypertension, or endocrine
disorder as determined by investigator.
5. Use of antipsychotic, antidepressant, or other prescription medications unless dose is
stable for at least 7 days prior to randomization.
6. Use of any investigational treatment within 30 days of randomization.
7. Current pregnancy.
8. Current lactation.
9. Previous allergic reaction to mifepristone or drugs of similar chemical structure.
10. Use of any oral contraceptives or other drugs that may result in adverse
drug-mifepristone interaction effects. A 30-day wash out period for oral
contraceptives is required before mifepristone begins.
Ages Eligible for Study
18 Years - 75 Years
Genders Eligible for Study