Efficacy and safety of sulforaphane for treatment of mild to moderate depression in patients with history of cardiac interventions: A randomized, double‐blind, placebo‐controlled clinical trial
Autor: | Kamyar Moradi, Amir Ashraf-Ganjouei, Fatemeh Ghazizadeh-Hashemi, Nazila Shahmansouri, Shahin Akhondzadeh, Sayna Bagheri, Maryam Mehrpooya, Ahmad Ali Noorbala |
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Rok vydání: | 2021 |
Předmět: |
Adult
Male medicine.medical_specialty medicine.medical_treatment Placebo chemistry.chemical_compound Percutaneous Coronary Intervention Double-Blind Method Isothiocyanates Internal medicine medicine Humans Depression (differential diagnoses) Aged Depression business.industry General Neuroscience Hamilton Rating Scale for Depression Repeated measures design Percutaneous coronary intervention General Medicine Middle Aged Clinical trial Psychiatry and Mental health Treatment Outcome Neurology chemistry Sulfoxides Conventional PCI Female Neurology (clinical) business Sulforaphane |
Zdroj: | Psychiatry and Clinical Neurosciences. 75:250-255 |
ISSN: | 1440-1819 1323-1316 |
DOI: | 10.1111/pcn.13276 |
Popis: | AIM Depression has been recognized as one of the disorders associated with cardiac interventions such as percutaneous coronary intervention (PCI) or coronary artery bypass graft surgery (CABG). In the present study, we evaluated the efficacy and safety of sulforaphane in treatment of depression induced by cardiac interventions. METHODS After initial screening, 66 patients with previous history of at least one cardiac intervention and current mild to moderate depression were randomly assigned to two parallel groups receiving either sulforaphane (n = 33) or placebo (n = 33) for six successive weeks. Efficacy was assessed using the Hamilton Rating Scale for Depression (HAM-D) at baseline and week 2, 4, and 6. Safety of the treatments was checked during the trial period. RESULTS Sixty participants completed the clinical trial (n = 30 in each group). Baseline demographic and clinical parameters were all similar among groups. Repeated measures analysis indicated that the sulforaphane group exhibited greater improvement in HAM-D scores throughout the trial (P |
Databáze: | OpenAIRE |
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