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Active clinical trials for "Dry Eye Syndromes"

Results 631-640 of 976

Acute Comfort and Blur Profile of a Lubricant Eye Drop Versus a Marketed Lubricant Eye Gel

Dry Eye

The purpose of this study is to compare the comfort and blurriness of an investigational lubricant eye drop with a marketed lubricant eye gel.

Completed3 enrollment criteria

Evaluation of the Repeated Usage of Systane Ultra Eyedrop

Dry Eye

Comparison of two contact lens solutions.

Completed19 enrollment criteria

Dose-response Study of OPC-12759 Ophthalmic Suspension

Dry Eye Syndromes

The purpose of this study is to evaluate the dose-response of OPC-12759 ophthalmic suspension in dry eye patients.

Completed13 enrollment criteria

Analysis of Postoperative Ocular Surface Changes and Intervention Effect After PPV in MGD Dry Eye...

Meibomian Gland Dysfunction of Unspecified EyeUnspecified Eyelid

AIM: To observe ocular surface changes after phacovitrectomy in patients with mild to moderate meibomian gland dysfunction (MGD)-type dry eye and track clinical treatment response using a Keratograph 5M and a LipiView interferometer. METHODS: Forty cases were randomized into control group A and treatment group B; the latter received meibomian gland treatment 3 days before phacovitrectomy and sodium hyaluronate before and after surgery. The average non-invasive tear film break-up time (NITBUTav), first non-invasive tear film break-up time (NITBUTf), non-invasive measured tear meniscus height (NTMH), meibomian gland loss (MGL), lipid layer thickness (LLT) and partial blink rate (PBR) were measured preoperatively and 1 week, 1 month and 3 months postoperatively.

Completed15 enrollment criteria

Study Evaluating the Safety and Efficacy of AR-15512

Dry Eye Disease

This will be a Phase 3, multicenter, vehicle-controlled, double-masked, randomized study conducted at approximately 20 sites in the United States. All subjects enrolled will have dry eye disease (DED). The study will consist of Screening (Day -14) and Baseline (Day 1) visits as well as visits at Day 7, Day 14, Day 28, and Day 90 (Study Exit).

Completed14 enrollment criteria

The Effect of SYSTANE® BALANCE on Tear Film Break Up Time in Dry Eye Subjects

Dry Eye

The purpose of this study was to evaluate the ability of SYSTANE® BALANCE dosed 4 times a day for 30 days to increase non-invasive tear film break up time over baseline, compared to a saline control, in dry eye subjects with lipid deficiency.

Completed16 enrollment criteria

The Effect of Electrical Stimulation on Tear Production

Dry Eye

The purpose of this study is to investigate whether electrical stimulation of the nerve innervating the tear gland results in tear production in subjects with severe Dry Eye.

Completed8 enrollment criteria

Treatment of Meibomian Gland Dysfunction Prior to Cataract Surgery

BlepharitisDry Eye Syndrome

The purpose of this pilot feasibility study is to assess whether treating meibomian gland dysfunction (MGD) prior to cataract surgery helps promote meibomian gland function, visual quality and ocular comfort after cataract surgery.

Completed11 enrollment criteria

Tear Lipid Layer Thickness With Emollient Eye Drops

Dry Eye Syndromes

Crossover comparison of lipid layer thickness with two artificial tear formulations

Completed15 enrollment criteria

Tear Film Innovations iLux Safety Study

Meibomian Gland DysfunctionEvaporative Dry Eye

The objective of this study was to measure the temperature of the cornea and surrounding eye tissue temperature immediately after heating the eyelids with the iLux device using the protocol treatment profile. Eligible participants attended one treatment visit, with follow-up one day following the procedure.

Completed8 enrollment criteria
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