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Continuous Intraocular Pressure (IOP) Monitoring in Pigmentary Dispersion Syndrome and Pigmentary Glaucoma Patients

NCT01253109 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2012-01-24

No results posted yet for this study

Summary

This study monitors the intraocular pressure (IOP) over 4 to 6 hours using the SENSIMED Triggerfish® device and Goldmann Applanation Tonometry (GAT) in pigment dispersion syndrome and pigmentary glaucoma patients. The aim of the study is to detect SENSIMED Triggerfish® output signal peak after induced fluctuation by physical exercise or pupil dilation.

Conditions

  • Pigmentary Dispersion Syndrome
  • Pigmentary Glaucoma Patients

Interventions

DEVICE

SENSIMED Triggerfish

Contact lens-based device for continuous IOP monitoring

Sponsors & Collaborators

  • Private practicioner, Dr Sunaric Mégevand

    collaborator UNKNOWN

  • Orasis, AugenZentrum Pajic

    collaborator UNKNOWN

  • Sensimed AG

    lead INDUSTRY

Principal Investigators

  • Gordana Sunaric Megevand, Dr · Private Practice

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2011-11-30
Completion
2011-11-30

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01253109 on ClinicalTrials.gov