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Partial Lacrimal Punctual Occlusion

NCT00802399 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2009-01-22

No results posted yet for this study

Summary

The purpose of this study is to describe a case series of patients with chronic dry eye submitted to partial punctual occlusion.

Conditions

  • Dry Eye

Interventions

PROCEDURE

Partial Lacrimal Punctual Occlusion

Cauterization of the edge of all lacrimal punctum was carried out in all patients

Sponsors & Collaborators

  • University of Sao Paulo General Hospital

    lead OTHER

Principal Investigators

  • Ricardo Holzchuh, MD · Instituto do Coracao

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-09-30
Primary Completion
2008-11-30
Completion
2008-11-30

Countries

  • Brazil

Study Locations

More Related Trials

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 NCT00802399 on ClinicalTrials.gov