Efficacy of Selective Laser Trabeculoplasty in Patients Under Treatment With Topical Prostaglandines
1 other identifier
observational
200
1 country
1
Brief Summary
Retrospective analysis of efficacy of selective laser trabeculoplasty in patients under treatment with topical prostaglandins compared to patients without topical prostaglandins is performed. Inclusion criterion are patients with glaucoma or ocular hypertension, who underwent treatment with selective laser trabeculoplasty due to insufficient control of intraocular pressure during their routine treatment at the University Hospital Zurich / Division of Ophthalmology.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2011
Longer than P75 for all trials
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
November 1, 2011
CompletedFirst Submitted
Initial submission to the registry
November 3, 2011
CompletedFirst Posted
Study publicly available on registry
November 8, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2015
CompletedJanuary 6, 2015
December 1, 2014
4.1 years
November 3, 2011
January 5, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
IOP
t0
Study Arms (2)
PGA
Patients under glaucoma treatment with prostaglandines
NON-PGA
Patient not recieving prostaglandines to treat their glaucoma
Interventions
trabeculoplasty with an SLT-Laser to reduce intraocular pressure
Eligibility Criteria
glaucoma patients
You may qualify if:
- Patients with ocular hypertension or glaucoma who underwent selective laser trabeculoplasty due to insufficient control of intraocular pressure despite maximum tolerated topical treatment.
You may not qualify if:
- Optic neuropathy other than glaucoma
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Zurich, Ophthalmic Clinic
Zurich, Canton of Zurich, 8091, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
01 Studienregister MasterAdmins
UniversitaetsSpital Zuerich
- PRINCIPAL INVESTIGATOR
Jens Funk, Professor, MD
University Hospital Zurich, Ophtalmic Clinic
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 3, 2011
First Posted
November 8, 2011
Study Start
November 1, 2011
Primary Completion
December 1, 2015
Study Completion
December 1, 2015
Last Updated
January 6, 2015
Record last verified: 2014-12