Partial Lacrimal Punctual Occlusion
PLPO
1 other identifier
interventional
37
1 country
1
Brief Summary
The purpose of this study is to describe a case series of patients with chronic dry eye submitted to partial punctual occlusion.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2008
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2008
CompletedFirst Submitted
Initial submission to the registry
December 3, 2008
CompletedFirst Posted
Study publicly available on registry
December 4, 2008
CompletedJanuary 22, 2009
August 1, 2008
2 months
December 3, 2008
January 21, 2009
Conditions
Keywords
Study Arms (1)
Partial Lacrimal Punctual Occlusion
OTHERCauterization of the edge of all lacrimal punctum was carried out in all patients
Interventions
Cauterization of the edge of all lacrimal punctum was carried out in all patients
Eligibility Criteria
You may qualify if:
- Sin and symptom of dry eye
- Use more than 4 times a day topic lubricant for the eye
You may not qualify if:
- Ocular diseases other than dry eye
- Use of systemic drugs
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo
São Paulo, São Paulo, 05403010, Brazil
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ricardo Holzchuh, MD
Instituto do Coracao
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
December 3, 2008
First Posted
December 4, 2008
Study Start
September 1, 2008
Primary Completion
November 1, 2008
Study Completion
November 1, 2008
Last Updated
January 22, 2009
Record last verified: 2008-08