RecruitingPhase 4NCT06587945

Nicotinamide Riboside Oral Supplementation in Macula Off Retinal Detachment

A Randomised Double-Masked Placebo-Controlled Trial of Nicotinamide Riboside Oral Supplementation in Macula Off Retinal Detachment


Sponsor

Center for Eye Research Australia

Enrollment

144 participants

Start Date

Sep 19, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Retinal detachment occurs when fluid separates the retina (a thin, light sensing tissue) from its usual attachment at the back of the eye. If detached, these retinal cells lose their normal blood supply and begin to die, which is the primary cause of vision loss in retinal detachment. The 'macula' refers to the very centre of the retina, with the highest density of retinal cells, most responsible for vision. Significant vision loss occurs when this part of the retina becomes separated (termed a 'macula-off retinal detachment'). Typically, surgery is required to repair the retinal detachment. Supporting the health of retinal cells at the macula may prolong their survival after detachment and their recovery postoperatively. Recent evidence has shown that boosting our nicotinamide adenine dinucleotide (NAD+) levels may improve the health of these cells and prolong their survival if detached. Oral Nicotinamide Riboside (NR) is converted into NAD+, and while not studied for macula-off retinal detachments, has been safely used in a range of other conditions. This study is designed to help evaluate the safety and tolerability of NR to help preserve vision in people diagnosed with macula-off retinal detachment. This study drug is given as an oral supplement (tablet) at the time of retinal detachment diagnosis, and daily for 20 weeks thereafter. The drug aims to prolong survival of cells in the retina (and macula) and their recovery after surgery. The long-term goal of this treatment is to reduce loss of vision after retinal detachment. The researchers will compare NR to a placebo (a look-alike substance that contains no drug) to see if NR has a positive effect on photoreceptor survival and quality of vision postoperatively. NR has been approved by the Therapeutic Goods Administration in Australia for many purposes but has not been approved for use in retinal detachment treatment.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Nicotinamide Riboside, Placebo, and others for people with retinal detachment. The study is currently recruiting participants at 5 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTNicotinamide Riboside

Oral Nicotinamide Riboside, 2g daily for 4 weeks followed by 1g daily for 16 weeks

OTHERPlacebo

Matched placebo

PROCEDUREVitrectomy and Gas tamponade

Standard of care Vitrectomy surgery for retinal reattachment


Locations(5)

Centre for Eye Research Australia

East Melbourne, Victoria, Australia

Cerulea

East Melbourne, Victoria, Australia

The Royal Victorian Eye and Ear Hospital

East Melbourne, Victoria, Australia

Dr David Fabinyi

Geelong, Victoria, Australia

Dr David Sousa

Geelong, Victoria, Australia

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NCT06587945


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