An Evaluation of Tangible Boost Replenishing System for Patients With Stevens Johnson Syndrome, Sjogren's Syndrome, and Graft Versus Host Disease
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Sponsor
- Enrollment
- 28
- Locations
- 2
- Primary Endpoint
- Tear break up time
Study Overview
Brief Summary
The goal of this research is to determine if the Tangible Boost system adequately replenishes the Hydra-PEG coating on the surface of a rigid contact lens.
Hydra-PEG is a coating for soft and rigid contact lens, primarily composed of polyethylene glycol-based hydrogel, which is covalently bound to the surface of a contact lens. The Hydra-PEG coating is intended to improve wettability and comfort with contact lenses and is currently FDA approved on a number of contact lenses. For patients with Stevens Johnson Syndrome (SJS) (SS), or Graft versus Host disease (GVHD), diminished efficacy of the Hydra-PEG coating can lead to significant decline in satisfaction with the lenses over time. This is a prospective study to evaluate the efficacy of Tangible Boost, a monthly conditioning solution, to replenish the Hydra-PEG coating on rigid gas permeable contact lenses for patients with SJS, GVHD, and SS. Outcomes from this patient population will be compared to patients with dry eye disease.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description
Test and placebo treatment kits will be randomized by the sponsor prior to sending to clinical site.
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Written Informed Consent has been obtained prior to any study-related procedures taking place
- •Written documentation has been obtained in accordance with the relevant county and local privacy requirements, where applicable
- •Male or female
- •18 years of age and older prior to the initial visit
- •Is a new or established wearer of PROSE lenses with optimized lens fit prior to enrollment in the study
- •Has been diagnosed with Dry Eye Syndrome, SJS, SS, or GVHD
- •In the opinion of the investigator, the subject has the ability to follow study instructions
- •In the opinion of the investigator, the subject has the ability to complete all study procedures and visits
Exclusion Criteria
- •aphakic (i.e., missing their natural lens inside the eye)
- •Is currently participating in any other type of eye-related clinical or research study
- •Is pregnant or nursing as reported by the subject
- •Has a condition or is in a situation which, in the investigator's opinion, may put the subject at significant risk, may confound study outcomes, or may significantly interfere with the subject's participation in the study.
- •Has a known and self-reported allergy to the following substances: polyethylene glycol, polyvinyl alcohol, triethanolamine, polyquaternium-1, or edetate disodium, which are components of the Tangible Boost and Hydra-PEG systems or care regimen.
- •Has had previous ocular surgery within the past 12 weeks
- •Adults unable to consent (including adults unable to read and understand English)
- •Individuals who are not yet adults (infants, children, teenagers)
- •Pregnant women
- •Prisoners
- •Employees of BostonSight
Outcomes
Primary Outcomes
Tear break up time
Time Frame: 6 months
Seconds required for tear film to begin to break up
Visual Acuity
Time Frame: 6 months
Snellan visual acuity
Ocular Surface Staining
Time Frame: 6 months
Sodium fluorescein staining will be used to evaluate ocular surface damage indicated by cell damage or death. Corneal staining will be scored using the Oxford grading scale.
Contact Lens Comfort
Time Frame: 6 months
OSDI plus additional specific questions
Secondary Outcomes
- Contact lens fit characteristics(6 months)