Glaucoma
Study register · detail RCT · Glaucoma · 2026

Single oral administration of dronabinol increases ocular blood flow in patients with glaucoma.

Clear benefit GRADE Moderate 0 citations
Samplen = 23 Pat.
DurationSingle oral administration with…
ControlPlacebo
EndpointONHBF
Blindingdoppelblind
DesignRCT
Cannabinoidthc
Max. dose10.0 mg
Routeoral
Key finding

A single dose of 10 mg dronabinol significantly increased optic nerve head blood flow by approximately 10-12% without effects on intraocular pressure or blood pressure.

Summary

n=23 patients with primary open-angle glaucoma (POAG), randomized double-blind cross-over dronabinol (5 mg vs. 10 mg) vs. placebo. 10 mg dronabinol significantly increased optic nerve head blood flow (ONHBF) (MA +10.8±20.6%, p=0.018; MV +12.0±24.8%, p=0.042; MT +11.0±22.6%, p=0.022 vs. placebo) up to 4 h post-administration, without affecting IOP or blood pressure (p>0.548). Vessel density in the superficial vascular plexus +6.7±14.7% (p=0.040 vs. 5 mg).

P
PopulationAdults with treated primary open-angle glaucoma (POAG), n=23, mean age 68 ± 7 years
I
InterventionOral dronabinol 5 mg or 10 mg (synthetic THC), single dose, cross-over
C
ControlPlacebo (single oral dose)
O
Outcome10 mg dronabinol significantly increased optic nerve head blood flow (MA: +10,8%, p=0,018; MV: +12,0%, p=0,042; MT: +11,0%, p=0,022 vs. placebo) up to 4 h after administration; no effect on IOP or mean arterial pressure (p>0,548)
Confidence in the evidence
Moderate

The third of four GRADE levels, the effect estimate is probably reliable.

Downgraded for
Imprecision
Quality profile
Sample size
Blinding Double-blind
Effect size Clear benefit
Citations / year
Authors
Lindner T, Pai V, Janku P, Hommer N, Hommer A, Abensperg-Traun M, Petric L, Schmetterer L, Garhofer G, Schmidl D
DOI 10.1111/aos.17573
Design: RCT
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Abstract
Purpose: Glaucoma is a leading cause of irreversible blindness globally, primarily driven by elevated intraocular pressure (IOP). Still, some patients progress despite significant IOP lowering, potentially due to impaired ocular blood flow. This study aimed to evaluate the effects of dronabinol, a synthetic tetrahydrocannabinol derivative, on ocular blood flow in primary open-angle glaucoma (POAG) patients. Methods: This randomized, double-masked, placebo-controlled, cross-over study included 23 patients with treated POAG (mean age 68 +/- 7 years). All participants received dronabinol (11 patients received 5 mg and 12 received 10 mg in a randomized fashion) on one study day and placebo on the other study day. The primary outcome was optic nerve head blood flow (ONHBF) measured by laser speckle flowgraphy. Mean blur rate was determined for the large vessel area (MV), the tissue area (MT) and the total ONH area (MA). Secondary outcomes included vessel densities assessed by optical coherence tomography angiography, IOP, and blood pressure. Results: Administration of 10 mg dronabinol significantly increased Onhbf (Ma: 10.8 +/- 20.6%, p = 0.018, MV: 12.0 +/- 24.8%, p = 0.042, and MT: 11.0 +/- 22.6%, p = 0.022, each vs. placebo) up to 4 h post-administration without affecting IOP or mean arterial pressure (p > 0.548 each). Additionally, a significant increase in vessel density in the superficial vascular plexus was found after administration of 10 mg dronabinol (6.7 +/- 14.7%, p = 0.040 vs. 5 mg). Conclusion: This pilot study demonstrates that systemic dronabinol enhances ONHBF in glaucoma patients, suggesting its potential as adjunct therapy for glaucoma by targeting vascular dysfunction. Further longitudinal studies are needed to explore its long-term impact on disease progression and visual field preservation. Trial Registration: ClinicalTrials.gov ID: NCT04596826.

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