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Conditioning Solution

Boost for Dry Eye Syndrome

N/A
Waitlist Available
Led By Karen Carrasquillo, OD, PhD
Research Sponsored by Tangible Science
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months

Summary

This trial will test whether Tangible Boost, a monthly conditioning solution, can replenish the Hydra-PEG coating on rigid gas permeable contact lenses for patients with SJS, GVHD, and SS.

Eligible Conditions
  • Dry Eye Syndrome
  • Graft-versus-Host Disease
  • Sjogren's Syndrome
  • Toxic Epidermal Necrolysis
  • Stevens-Johnson Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Contact Lens Comfort
Ocular Surface Staining
Tear break up time
+1 more
Secondary study objectives
Contact lens fit characteristics

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: BoostExperimental Treatment1 Intervention
Subjects will use the Tangible Boost treatment on their lenses monthly throughout the study.
Group II: PlaceboPlacebo Group1 Intervention
Subjects will use a Placebo treatment (saline) on their lenses monthly throughout the study.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tangible Boost
2017
N/A
~40

Find a Location

Who is running the clinical trial?

Tangible ScienceLead Sponsor
2 Previous Clinical Trials
56 Total Patients Enrolled
Boston SightOTHER
5 Previous Clinical Trials
63 Total Patients Enrolled
Karen Carrasquillo, OD, PhDPrincipal InvestigatorBoston Sight
~9 spots leftby Nov 2025
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