Scleral Contact Lens Insertion Solution Study

NACompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

November 27, 2017

Primary Completion Date

November 30, 2018

Study Completion Date

November 30, 2018

Conditions
Irregular; Contour of Cornea
Interventions
DEVICE

contact lens insertion solution

"This contact lens solution is being tested for safety and comfort and is not an intervention. Subjects will have their scleral contact lenses filled with the test saline in the examination room and applied to their eyes. They will be monitored for symptoms and will be examined. Six to 8 hours later or whenever their lens clouding typically occurs they will return for further assessment and dispensing of solution if acceptable. subjects will use the solution for 5-9 days and return for a follow-up appointment. At each visit, subjects will complete an OSDI questionnaire and a Current Symptoms questionnaire."

Trial Locations (1)

43210

The Ohio State University College of Optometry, Columbus

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Contamac Ltd

INDUSTRY

lead

Jennifer Fogt

OTHER