drugset / Trial / NCT04036968
Enhancing Medication-based Analgesia in Humans- STUDY 2
Phase 2
Completed
31 enrolled
Johns Hopkins University
National Institute on Drug Abuse (NIDA) · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |