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Safety and Efficacy of Punctal Plug Insertion in Patients With Dry Eye

NCT01684436 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2019-04-17

Study results available
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Summary

This study will access changes in tear protein levels and symptoms of dry eye following insertion of a punctal plug.

Conditions

  • Dry Eye

Interventions

DEVICE

Punctal Plug

Punctal plugs inserted into the study eye on Day 1.

Sponsors & Collaborators

  • Allergan

    lead INDUSTRY

Principal Investigators

  • Medical Director · Allergan

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-10-01
Primary Completion
2013-07-31
Completion
2013-07-31

Countries

  • Singapore

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 NCT01684436 on ClinicalTrials.gov