Possibia

5273385

Last Update Posted: 2023-11-18

Recruiting

All Genders

accepted

18 Years +

40 Estimated Participants

No Expanded Access

Interventional Study

Does not accept healthy volunteers

Efficacy of the Nanodropper Device on Intraocular Pressure in Patients With Glaucoma

Glaucoma is the leading cause of irreversible blindness worldwide. Previous studies demonstrate that smaller eye drops used in the treatment of glaucoma are just as efficacious as their larger counterparts. The proposed study hopes to demonstrate the non-inferiority of using Nanodropper to lower intraoccular pressure (IOP) in glaucoma patients compared to standard of care eye drops.

The proposed study strives to demonstrate the non-inferiority of using Nanodropper to lower IOP in glaucoma patients compared to standard of care (SOC) eye drops in a randomized trial.

Primary Aim: Demonstrate non-inferiority of using Nanodropper to lower IOP compared to standard of care eye drops in glaucoma patients.

Stable glaucoma participants and ocular hypertension participants of ages 18+ will be randomized to either use Nanodropper for eye drop administration in both eyes OR administer drops regularly (standard of care) in both eyes. Participants will be followed-up at 1 month and 3 months.

Eligibility

Relevant conditions:

Glaucoma

Ocular Hypertension

Open Angle Glaucoma

If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.

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Contact Information

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Data sourced from ClinicalTrials.gov