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

NCT01854905 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2014-03-14

Study results available
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Summary

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.

Conditions

  • Dry Eye Syndromes

Interventions

OTHER

No Treatment

Patients attending consultation for LASIK on Day 1. No intervention or treatment is administered during the study.

Sponsors & Collaborators

  • Allergan

    lead INDUSTRY

Principal Investigators

  • Medical Director · Allergan

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • Russia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01854905 on ClinicalTrials.gov