drugset / Trial / NCT02548559

Sublingual Cannabidiol for Anxiety

NCT02548559 ↗

Phase 2 Completed 46 enrolled Staci Gruber, Ph.D.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is an open-label to double-blind study evaluating the effects of cannabidiol (CBD) for the treatment of anxiety in adults. Participants will use a sublingual (under-the-tongue) solution of whole plant-derived CBD or placebo three times daily for four weeks in addition to their normal treatment regimen. Participants' clinical state will be assessed weekly during the treatment period. In addition, cognitive function and measures of quality of life, sleep, and general health will be assessed at baseline and the post-treatment final visit.

Timeline

Start
2018-08-14
Primary completion
2025-03-13
Completion
2025-03-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Cannabidiol Other / unclassified 10 mg Other

Indications