← Eichor
Study identifier: NCT07696871 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Cannabidiol Oil for Treatment-Resistant Major Depression

Condition: Major Depressive Disorder (MDD) · Treatment-resistant Depression (TRD)  ·  Sponsor: Universidade do Sul de Santa Catarina

PhasePhase 1/Phase 2
Planned participants120
Who can joinAll sexes, 18 Years to 69 Years
Healthy volunteersNo

About this study

Major depressive disorder is one of the leading causes of disability worldwide, and a substantial proportion of patients do not achieve adequate improvement with conventional antidepressant treatments. Cannabidiol (CBD), a non-intoxicating cannabinoid derived from Cannabis sativa, has shown potential anxiolytic, anti-inflammatory, and neurobiological effects that may be relevant for depressive disorders. The ANANDA trial is a multicenter, randomized, double-blind, placebo-controlled clinical trial designed to evaluate the efficacy, safety, and tolerability of full-spectrum cannabidiol oil as an adjunctive treatment in adults with treatment-resistant major depressive disorder. A total of 120 participants will be randomly assigned to receive either full-spectrum cannabidiol oil or placebo for 12 weeks while maintaining stable antidepressant treatment. Clinical assessments of depressive symptoms, anxiety, sleep quality, perceived stress, and adverse effects will be performed at baseline, Week 4, and Week 12. Blood samples will be collected at baseline and after 12 weeks to investigate inflammatory and neuroendocrine biomarkers. The primary objective is to evaluate changes in depressive symptoms after 12 weeks of treatment. Secondary objectives include the assessment of anxiety, sleep quality, perceived stress, biological markers, safety, and tolerability. The findings of this study may contribute to the development of new therapeutic approaches for treatment-resistant depres…

This description comes directly from the study's public registry record.

Talk to the study team

Rafael Mariano Bitencourt, PhD  ·  +55 48 9 8833-6460  ·  bitencourtrm@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Universidade do Sul de Santa Catarina - UNISULTubarão, Santa Catarina, BrazilRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07696871