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

This study is enrolling participants by invitation only.
Sponsor:
Information provided by (Responsible Party):
University of Zurich
ClinicalTrials.gov Identifier:
NCT01467440
First received: November 3, 2011
Last updated: January 5, 2015
Last verified: December 2014

November 3, 2011
January 5, 2015
November 2011
December 2015   (final data collection date for primary outcome measure)
IOP [ Time Frame: t0 ] [ Designated as safety issue: No ]
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Complete list of historical versions of study NCT01467440 on ClinicalTrials.gov Archive Site
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Efficacy of Selective Laser Trabeculoplasty in Patients Under Treatment With Topical Prostaglandines
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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.

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Observational
Observational Model: Case Control
Time Perspective: Retrospective
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Non-Probability Sample
glaucoma patients
  • Glaucoma
  • Ocular Hypertension
Device: Selective Laser Trabeculoplasty
trabeculoplasty with an SLT-Laser to reduce intraocular pressure
Other Name: SLT-Laser, Tango Laser, Ellex Medical Pty. Ltd., 82 Gilbert Street, Adelaide, SA 5000 Australia
  • PGA
    Patients under glaucoma treatment with prostaglandines
    Intervention: Device: Selective Laser Trabeculoplasty
  • NON-PGA
    Patient not recieving prostaglandines to treat their glaucoma
    Intervention: Device: Selective Laser Trabeculoplasty
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Enrolling by invitation
200
December 2015
December 2015   (final data collection date for primary outcome measure)

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
Both
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Switzerland
 
NCT01467440
SLT_PG_2011
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University of Zurich
University of Zurich
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Study Director: 01 Studienregister MasterAdmins UniversitaetsSpital Zuerich
Principal Investigator: Jens Funk, Professor, MD University Hospital Zurich, Ophtalmic Clinic
University of Zurich
December 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP