About this trial
This randomized controlled trial aims to evaluate the clinical efficacy of intradermal acupuncture as an adjunctive intervention to assist selective serotonin reuptake inhibitor (SSRI) dose reduction or discontinuation in adult patients with major depressive disorder (MDD). Participants receiving SSRIs and planning gradual dose reduction or discontinuation will be randomly assigned to one of three groups: SSRI tapering alone, sham intradermal acupuncture plus SSRI tapering, or intradermal acupuncture plus SSRI tapering. Clinical outcomes and autonomic nervous system function will be assessed to determine the effectiveness and potential mechanisms of intradermal acupuncture in facilitating SSRI reduction and alleviating withdrawal-related symptoms.
Eligibility criteria
Qualifiers
Adults aged 18-60 years
Disqualifiers
Severe uncontrolled primary medical conditions
Trial design
Treatments tested in this trial
- Selective Serotonin Reuptake Inhibitors (SSRIs)
- Sham Intradermal Acupuncture
- Intradermal Acupuncture