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NCT01467440 Clinical Trial

Efficacy of Selective Laser Trabeculoplasty in Patients Under Treatment With Topical Prostaglandines

Glaucoma Clinical Trial

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT01467440
Other study ID # SLT_PG_2011
Secondary ID
Status Enrolling by invitation
Phase Phase 4
First received November 3, 2011
Last updated January 5, 2015
Start date November 2011
Est. completion date December 2015

Study information
Verified date December 2014
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 200
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- Patients with ocular hypertension or glaucoma who underwent selective laser trabeculoplasty due to insufficient control of intraocular pressure despite maximum tolerated topical treatment.

Exclusion criteria:

- Optic neuropathy other than glaucoma

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Device:
• Selective Laser Trabeculoplasty
trabeculoplasty with an SLT-Laser to reduce intraocular pressure

Locations
Country Name City State
Switzerland University Hospital Zurich, Ophthalmic Clinic Zurich ZH

Sponsors (1)
Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary IOP t0 No
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