| Trial Acronym | DREAM |
| Trial Title | Determining the Role of Synthetic Cannabinoids in Eye Pressure And Tolerability Measurements (DREAM) |
| Clinical Area | Ophthalmology |
| Trial Status | Open to Recruitment |
| Trial Registration | ISRCTN10996483: Determining the role of synthetic cannabinoids in eye pressure and tolerability measurements |
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Recruitment
Recruitment Target 10 Date Open to Recruitment 8th July 2026 Recruitment Date Closed to Recruitment -
Trial Design
Trial Design A pilot, randomised, double-masked, placebo-controlled, single site, cross-over trial Study Aim Aim The study aims to assess the preliminary efficacy and safety of a peripherally selective, synthetic cannabinoid (ART27.13), given orally, to reduce intraocular pressure (IOP) in patients with ocular hypertension or early primary open angle glaucoma
Objectives
- To evaluate the IOP lowering efficacy of ART27.13
- To assess the safety and tolerability of ART27.13
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Chief Investigator (CI)
Chief Investigator Professor Augusto Azuara-Blanco, Queen’s University Belfast -
Sponsor(s) & Funder(s)
Sponsor Belfast Health & Social Care Trust Funder Glaucoma UK Public Health Agency (PHA), Health and Social Care (HSC) Research & Development Division, Northern Ireland
