Dry Eye Clinical Trial
Official title:
Tangible Hydra-PEG: A Promising Solution for Scleral Lens Wearers With Dry Eye
Tangible Hydra-PEG is a novel coating technology designed to improve lens wettability, deposit resistance, and tear film breakup time. This is a randomized double masked cross-over study to examine contact lens discomfort and dry eye symptoms with Tangible Hydra-PEG treated scleral lens wear compared to untreated scleral lens wear in the dry eye patient population.
Dry eye (DE) is a common complaint of millions of people worldwide with a significant impact
on quality of life. For decades, this condition has presented a challenge to eye care
professionals as conventional therapies are often ineffective. Recently, scleral lenses have
demonstrated to be a promising therapeutic and vision rehabilitative option for dry eye
sufferers. Nonetheless, despite the benefits of scleral lenses for dry eye patients,
inadequate wettability of scleral lenses with subsequent diminished comfort and visual
clarity remains a concern for scleral lens wearers with dry eye.
Tangible Hydra-PEG (Tangible Science LLC, Menlo Park, CA, USA) is a novel coating technology
designed to improve lens wettability, deposit resistance, and tear film breakup time,
ultimately enhancing contact lens comfort. While studies have shown that Tangible Hydra-PEG
technology can improve contact lens discomfort (CLD) in soft contact lens and gas permeable
lens wearers, to our knowledge, no clinical research investigation has examined the benefits
of this new coating on scleral lens wear in dry eye sufferers. As such, the aim of this study
is to compare the CLD and DE symptoms of dry eye scleral lens wearers between Tangible
Hydra-PEG treated scleral lens wear and untreated scleral lens wear. CLD and DE signs will
also be assessed to corroborate our findings.
This will be the first randomized double masked cross-over study to examine CLD and DE
symptoms of Tangible Hydra-PEG treated scleral lens wear compared to untreated scleral lens
wear in the dry eye patient population. Tangible Hydra-PEG treated scleral lenses can
potentially minimize CLD and DE symptoms, ultimately improving outcomes for patients coping
with dry eye disease. This study will provide new information about this innovative
technology and help practitioners envisage rehabilitative options which will best optimize
the quality of life of this important patient population.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05027087 -
The Effect of a Novel Blueberry Supplement on Dry Eye Disease
|
Phase 3 | |
Completed |
NCT05102409 -
An Exploratory Clinical Trial to Assess Safety and Tolerability in Subjects With Dry Eye Disease
|
Phase 2 | |
Completed |
NCT06159569 -
Performance and Tolerability of the Medical Device LACRIACT
|
N/A | |
Completed |
NCT04081610 -
Clinical Trial to Evaluate the Safety and Tolerability of Lagricel® Ofteno Multi-dose Ophthalmic Solution
|
Phase 1 | |
Completed |
NCT05062564 -
Efficacy of LipiFlow in Patients Affected by Meibomian Gland Dysfunction in Reducing Post-cataract Surgery Dry Eye
|
N/A | |
Completed |
NCT05825599 -
PMCF Study to Evaluate Performance and Safety of "HPMC-based Eyedrops" Used to Relieve Dry Eye Symptoms
|
N/A | |
Completed |
NCT03418727 -
Dry Eye Disease Study With Brimonidine
|
Phase 2 | |
Active, not recruiting |
NCT04425551 -
Effect of Micropulse Laser on Dry Eye Disease Due to Meibomian Gland Dysfunction
|
N/A | |
Recruiting |
NCT04527887 -
Intracanalicular Dexamethasone Insert for the Treatment of Inflammation and Discomfort in Dry Eye Disease (DEcIDED)
|
Phase 4 | |
Not yet recruiting |
NCT06379685 -
Study to Evaluate the Safety and Tolerability of PRO-190 Ophthalmic Solution Compared to Systane Ultra® on the Ocular Surface.
|
Phase 1 | |
Active, not recruiting |
NCT05618730 -
Safety, Tolerability, Plug Retention and Preliminary Efficacy of Tacrolimus-loaded Punctal Plug in Patients With Moderate to Severe Dry Eye Disease - Cohort B
|
Phase 1 | |
Completed |
NCT04553432 -
Dry Eye OmniLenz Application of Omnigen Research Study
|
Phase 4 | |
Recruiting |
NCT04109170 -
Dry Eye Evaluation System Based on Bioinformatics
|
||
Completed |
NCT04105842 -
Refitting Daily Disposable Contact Lens Wearers With Dry Eye Disease With A Different Daily Disposable Lens Type
|
N/A | |
Completed |
NCT05505292 -
Lifitegrast 5% for the Treatment of Dry Eye In Habitual Soft Contact Lens Wearers
|
Phase 4 | |
Completed |
NCT04668131 -
Study on Curative Effect and Mechanism of Acupuncture on Neuropathic Pain in Dry Eye Disease
|
N/A | |
Completed |
NCT06176651 -
Evaluation of Miebo (Perfluorohexyloctane) Eyedrops in Habitual Contact Lens Wearers
|
Phase 4 | |
Not yet recruiting |
NCT02218827 -
Topical Steroid Treatment For Dry Eye
|
N/A | |
Completed |
NCT02235259 -
Efficacy and Safety of XG-104 for the Treatment of Dry Eye
|
Phase 2 | |
Completed |
NCT01959854 -
Efficacy of Topical 0.2% Xanthan Gum in Patients With Dry Eye
|
N/A |