Lacritin and Heparanase Levels in Human Tears After Laser Refractive Surgery

Fort Belvoir Community Hospital

Status

Completed

Conditions

Myopia

Treatments

Other: Tear collection

Study type

Observational

Funder types

Other

Other U.S. Federal agency

Identifiers

NCT01049724

351515

Details and patient eligibility

About

The purpose of this study is to measure tear lacritin and heparanase levels before and following surgery using a minimal risk procedure to collect tears from patients undergoing PRK or LASIK.

Full description

Lacritin is a naturally occurring tear protein with antimicrobial activity that is capable of stimulating mitogenesis in human corneal epithelial cells and promoting production of tears in lacrimal gland acinar cells. A recently developed immunoassay for lacritin may help characterize the lacritin response following refractive surgery with the possible development of recombinant lacritin as a novel therapeutic agent for wound healing. Heparanase (HPSE) acts as a regulator for lacritin by cleaving heparan sulfate chains and allowing lacritin to bind. We aim to measure both tear lacritin and HPSE pre- and post-operatively to elucidate lacritin and HPSE's response in patients undergoing PRK (photorefractive keratectomy) and LASIK (Laser-assisted in situ keratomileusis) at the Walter Reed Center for Refractive Surgery.

Enrollment

196 patients

Sex

All

Ages

21 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Active duty US Army Soldiers eligible for care at FBCH
Undergoing PRK or LASIK
Male or female, of any race, and at least 21 years old and not older than 55 years old at the time of the tear collection. The lower age limit of 21 years is intended to ensure documentation of refractive stability.
Appropriately aged individuals who report that their eyes are "normal" and who have no active eye illness as determined by the principal investigator or sub-investigator.
Ability and willingness to understand and provide informed consent to participate in this study.
Up to -10.00 diopters of myopia.
Subject must expect to be located in the greater Washington DC area for a 12 month period post-operatively.
Consent of the subject's command (active duty) to participate in the study.
Access to transportation to meet follow-up requirements.

Exclusion criteria

Any reason to be excluded for PRK or LASIK
Female subjects who are pregnant, breast-feeding or intend to become pregnant during the study. Female subjects will be given a urine pregnancy test prior to participating in the study to rule out pregnancy. [Pregnancy and breastfeeding are contraindications to refractive surgery in general, including PRK, whether participating in this study or not]
Patients with known sensitivity or inappropriate responsiveness to any of the medications used in the post-operative course.
Any physical or mental impairment that would preclude participation in any of the examinations.
Anterior basement membrane dystrophy
History of recurrent epithelial erosion
Significant dry eye (symptomatic with Schirmer <5mm at 5 minutes)
Other corneal epithelial disorder or healing abnormality
Individuals with any infectious or inflammatory ocular conditions (e.g. have "pink eye" or uveitis).
Individuals diagnosed with dry eye or other ocular surface condition, including but not restricted to neurotropic keratitis, anterior basement membrane dystrophy, and recurrent corneal erosions.