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Risk Factors of Hypertensive Phase after Glaucoma Drainage Devices Implantatio

Not Applicable
Recruiting
Conditions
Increase intraocular pressure
Risk Factors
Hypertensive Phase
Glaucoma drainage devices
Glaucoma
Registration Number
TCTR20151214001
Lead Sponsor
one
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

•Glaucoma patients underwent Glaucoma drainage devices implantation at King Chulalongkorn Memorial Hospital during January 2003 to January 2015

Exclusion Criteria

•Follow up period less than 12 months
•Intraocular pressure (IOP) rising caused by tube obstruction, retraction, or valve malfunction

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Risk factors of hypertensive phase 12 months Prevalence of factors found by reviewing chart
Secondary Outcome Measures
NameTimeMethod
Rate of hypertensive phase 12 months Prevalence of the events found by reviewing chart,surgical outcome at 12 months 12 months Prevalence of surgical failure found by reviewing chart
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