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An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusis (LASIK) Therapy

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Allergan

Status

Completed

Conditions

Dry Eye Syndromes

Treatments

Other: No Treatment

Study type

Observational

Funder types

Industry

Identifiers

NCT01854905
MAF-AGN-OPH-DE-015

Details and patient eligibility

About

This is an observational, study of dry eye in patients at the consultation visit prior to LASIK surgery. There is no treatment administered or intervention during the study.

Enrollment

400 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Attending an ophthalmology consultation for LASIK

Exclusion criteria

  • None

Trial design

400 participants in 1 patient group

Patients Attending Consultation for LASIK
Description:
Patients attending consultation for LASIK on Day 1. No intervention or treatment is administered during the study.
Treatment:
Other: No Treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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