Examination of a Soy-Based Supplement for Major Depression

Completed · Phase 2

Conditions studied: Depression

In brief

The purpose of this study is to find out if the soy-based dietary supplement Novasoy (Registered Trademark) is effective for the short-term treatment of clinical depression. This study will also evaluate whether Novasoy (Registered Trademark) is effective in treating the anxiety that often accompanies depression and will assess the best dose level. Novasoy (Registered Trademark) is a marketed botanical dietary supplement containing soy isoflavones. The active form of the soy isoflavone genistin may be a novel treatment for neuropsychiatric illnesses. The soy isoflavone's specific hormonal properties may also have beneficial effects on brain function in depressed patients. This study will be conducted in two phases. During Phase I, participants will stop all medications for at least 1 week. A psychiatric and medical examination will be conducted. During Phase II, participants will be randomly assigned to receive either Novasoy (Registered Trademark) or a placebo (an inactive pill) for 8 weeks. Participants who do not respond to treatment after 5 weeks will be given a higher dose of their assigned medication. After the 8-week period, participants will be monitored for up to 3 months before being referred back to their clinician for further treatment.

Key facts

Study ID

NCT00042380

Run by

National Institute of Mental Health (NIMH)

People needed

120

Starts

2002-07-01

Expected to finish

2005-04-01

Last updated by the study team

2008-03-04

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects may be included in the study only if they meet all of the following criteria:
• Male or female subjects, 18 or older.
• Female subjects of childbearing potential must be using a medically accepted means of contraception as defined by one of the following: a) A barrier method of contraception. A barrier method of contraception is a physical barrier designed to prevent pregnancy, i.e., contraceptive foam or suppositories, spermicides, condoms, or diaphragm. b)Oral contraceptives, estrogen/progesterone-based or progesterone based. Women of childbearing potential also must have a negative serum beta-HCG at prestudy.
• Each subject must have a level of understanding sufficient to agree to all tests and examinations required by the protocol.
• Each subject must understand the nature of the study and must sign an informed consent document.
• Subjects must fulfill the criteria for major depression without psychotic features as defined in DSM-IV based on clinical assessment and confirmed by structured diagnostic interview SCID-P.
• Subjects must have a score at Visit 1 and Visit 2 of at least 20 on the MADRS (within 20%) and CGI-S greater than or equal to 3.

You may not qualify if…

• Participation in a clinical trial of another investigational drug within 1 month (30 days) prior to study entry (Visit 1).
• Female subjects who are either pregnant or nursing.
• Patients initiating hormonal treatment (e.g., estrogen) in the last 3 months for mood, perimenopausal, or menstrual symptoms (OCP for birth control are acceptable but should not have been started in the last 2 month).
• Women ages 40-55 with irregular periods, or last menstrual period within the last 12 months, AND laboratory evidence confirming possible perimenopause, FSH greater than 14 IU/L.
• Serious, unstable illnesses including hepatic, renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease), endocrinologic, neurologic, immunologic, or hematologic disease.
• History of malignancies or neoplastic disorders.
• Any present or past history of breast carcinoma, or any woman with a family history of the following: premenopausal breast cancer or bilateral breast cancer in a first-degree relative; multiple family members (greater than 3 relatives) with postmenopausal breast cancer.
• History of porphyria.
• History of pulmonary embolus or thrombophlebitis.
• Women with a history of endometriosis, pelvic lesions, ovarian enlargement, or abnormal vaginal bleeding.
• Subjects with uncorrected hypothyroidism or hyperthyroidism.
• Subjects with one or more seizures without a clear and resolved etiology.
• Documented history of hypersensitivity to soy products.
• DSM-IV substance abuse (except nicotine and caffeine) within the past 90 days and substance dependence within the past 12 months.
• Treatment with a reversible monoamine oxidase inhibitor, guanethidine, or guanadrel within 2 week prior to Visit 2.
• Treatment with fluoxetine within 2 weeks prior to Visit 2.
• Treatment with any other concomitant medication with primarily CNS activity, other than specified in the Appendix.
• Current diagnosis of schizophrenia or other psychotic disorder as defined in the DSM-IV.
• Known allergy to soy or soy constituents.
• Judged suicidal risk based on use of the HAM-D suicide item greater than or equal to 3.
• Patients will not be allowed to receive a new course of structured psychotherapy during the trial.
• Patients will be excluded who have previously failed greater than 3 antidepressant trials by ATHF criteria.
• Patients will be excluded who have had ECT in the past 12 weeks.

Where it is running

• National Institute of Mental Health (NIMH) — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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