Sertraline Compared With Hypericum Perforatum (St.John's Wort) in Treating Depression

Completed · Phase 3

Conditions studied: Depression, Unspecified Adult Solid Tumor, Protocol Specific

In brief

RATIONALE: Antidepressants such as sertraline and the herb hypericum perforatum (St. John's wort) may be effective in treating mild to moderate depression. It is not yet known which treatment is more effective in improving depression in patients who have cancer. PURPOSE: This randomized phase III trial is studying how well sertraline works compared to St. John's wort in treating mild to moderate depression in patients with solid tumors.

Key facts

Study ID

NCT00066859

Run by

Wake Forest University Health Sciences

People needed

2

Starts

2004-03-01

Expected to finish

2005-11-01

Last updated by the study team

2021-09-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Mild or moderate depression as determined by the following criteria (see Section 7.1 and 8.0)
• Mild : HRSD score 10-14; moderate: HRSD score 15-19 (Appendix IV)
• At least 2 of nine symptoms of depression on the PHQ (Appendix V)
• At least one of the nine PHQ symptoms must be either depressed/irritable mood or anhedonia
• Histologically or cytologically documented solid tumor, lymphoma, or primary or metastatic brain tumor > 6 months from radiation with stable disease or no evidence of disease.
• Concurrent cancer chemotherapy with sertraline or St. John's wort is not allowed, therefore patients must have no plan for chemotherapy for 4 months
• Prior chemotherapy is allowed, but patients must be >4 weeks from prior chemotherapy except >6 weeks from prior mitomycin-C or nitrosourea
• Patients receiving Rituxin, Herceptin, Erbitux, Interferon, etc. are eligibile for this study while under treatment.
• Prior or concurrent radiation is allowed except brain irradiation for brain metastases or primary brain tumor. Must be > 6 months from radiation with stable disease or no evidence of disease.
• Age > 18 years
• ECOG performance status 0 -1 (Appendix III)
• Life expectancy >4 months
• Required initial laboratory values (within 3 days of registration): hemoglobin >10 g/dl and bilirubin <1.5 mg/dl, negative pregnancy test
• Signed protocol specific informed consent prior to registration
• Patient recruitment this study will be done through the out patient clinic. The research PI or designee including clinic physician, resident, research nurse or research assistant will review medical information to determine or verify protocol eligibility either at the time the patient is being seen in the clinic for a routine visit/consult or prior to the patient's clinic visit.

You may not qualify if…

• A patient will be excluded if he/she is (a) judged to be severely depressed using the following criteria: HRSD score 20 or more or a positive score on PHQ item i (suicidal ideation) or (b) judged not to be depressed by a score of 9 or less on the HRSD or fewer than two PHQ items scored positively. A patient who is found to be severely depressed or suicidal, either on initial screening or during the trial will be referred for appropriate treatment.
• Psychotic symptoms, dementia, marked agitation requiring medication
• Current or previous alcohol or drug dependence
• Hematologic malignancy (i.e., leukemias, multiple myeloma)
• Planned chemotherapy in the next 4 months
• Antidepressant or St. John's wort use in the last 4 weeks
• Current or planned use of erythropoietin (Procrit®, Aranesp®)
• Current or planned use of theophylline, warfarin (except for central line prophylaxis), protease inhibitors used to treat AIDS, digoxin, cyclosporin, benzodiazepines (such as diazepam, alprazolam, etc), calcium-channel blockers (such as diltiazem, nifedipine, etc), coenzyme A reductase inhibitors (cholesterol lowering agents), macrolide antibiotics (such as azithromycin, erythromycin, clarithromycin, etc), griseofulvin, phenobarbital, phenytoin, rifampin, rifabutin, ketoconazole, fluconazole, itraconazole, corticosteroids, grapefruit juice, or other naturopathic/herbal products that could interfere with St. John's wort (call study chairman with questions).
• Pregnant or nursing women

Where it is running

• Bay Area Tumor Institute — Oakland, California, United States
• Regional Radiation Oncology Center at Rome — Rome, Georgia, United States
• CCOP - Central Illinois — Decatur, Illinois, United States
• CCOP - Southeast Cancer Control Consortium — Goldsboro, North Carolina, United States
• High Point Regional Hospital — High Point, North Carolina, United States
• Comprehensive Cancer Center at Wake Forest University — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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