Clinical Trial of OCT-based Scleral Lens Fitting With Wide-Field OCT

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The purpose of this study is to see if OCT technology can optimize scleral contact lens fittings. Subjects with keratoconus, post-penetrating keratoplasty (PK), post-LASIK ectasia, post-radial keratotomy (RK), or a variety of anterior surface disorders requiring scleral lens fittings will be considered for enrollment. For each study eye, a clinically-selected scleral lens fit will be compared against an OCT-selected lens fit. The quality of each lens fit will be determined by flourescein exam at the slit lamp. Apical clearance, limbal clearance, conjunctival compression, and lens edge lift will be assessed. A lens that satisfies all four criteria will be considered satisfactory.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Eyes requiring fit for scleral lenses for KCN, post-PK, post-RK, post-LASIK ectasia, or various anterior surface disorders

Locations
United States
Oregon
Oregon Health & Science University, Casey Eye Institute
RECRUITING
Portland
Contact Information
Primary
Humberto Martinez, COT
martinhu@ohsu.edu
503-494-7712
Backup
Denzil Romfh, OD
romfhd@ohsu.edu
503-494-4351
Time Frame
Start Date: 2020-09-23
Estimated Completion Date: 2028-12
Participants
Target number of participants: 258
Treatments
Clinically-Selected Scleral Lens
The clinically-selected lens is based on slit lamp assessment. This lens will be compared against an OCT-selected lens.
OCT-Selected Scleral Lens
The OCT-selected lens is based on OCT measurements. This lens will be compared against a clinically-selected lens.
Related Therapeutic Areas
Sponsors
Collaborators: National Eye Institute (NEI)
Leads: Oregon Health and Science University

This content was sourced from clinicaltrials.gov