A Study to Evaluate Fogging in Scleral Contact Lens

Overview

About this study

The purpose of this study is to quantify potential decreases in visual acuity experienced by patients who experience mid-day fogging during scleral lens wear, compare severity of subjectively reported fogging with clinical findings, and to explore the relationship between scleral lens fitting parameters and mid-day fogging.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Please contact the study team to discuss whether or not you are eligible to participate in a study.

Inclusion Criteria:

  • Age 18 or older.
  • Scleral lens wearers with a history of 6 months of at least 5 hours of scleral lens wear at least 5 days/week are invited to participate.

Exclusion Criteria: 

  • Patients with active infections or unstable inflammation of the eyes are not eligible to participate.
  • Patients who have been refit into a different scleral lens design during the past 6 months.
  • Patients who are actively participating in the scleral lens fitting process.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Muriel Schornack, O.D.

Open for enrollment

Contact information:

Ophthalmology Research Study Coordinator

(507)284-5833

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

.
CLS-20472683

Mayo Clinic Footer