drugset / Trial / NCT04036968

Enhancing Medication-based Analgesia in Humans- STUDY 2

NCT04036968

NaSingle-groupTriple-blindBasic science

Summary

This is a single-group, within-subject, double-blind, double-dummy, placebo and active-controlled study evaluated whether the FDA-approved cannabinoid cannabidiol (CBD; Epidiolex) would enhance analgesia, subjective reports, and cognitive performance when compared to the FDA-approved opioid hydromorphone (Dilaudid). This is study 2 is a series of studies.

Timeline

Start
2020-02-01
Primary completion
2022-11-01
Completion
2022-11-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cannabidiol Other / unclassified 50 mg Oral
Subject Cannabidiol Other / unclassified 100 mg Oral
Subject Cannabidiol Other / unclassified 200 mg Oral
Subject Hydromorphone Other / unclassified 4 mg Oral