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Water Drinking Test During Intraocular Pressure Fluctuation (IOP) Monitoring

NCT01362868 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2011-11-09

No results posted yet for this study

Summary

The purpose of this study is to investigate the investigational device capacity to detect an intraocular pressure increase (IOP)induced by water intake.

Conditions

  • Healthy Subjects

Interventions

DEVICE

SENSIMED Triggerfish®

Soft contact lens-based device for the continuous monitoring of IOP fluctuations

Sponsors & Collaborators

  • Sensimed AG

    lead INDUSTRY

Principal Investigators

  • André Mermoud, MD · Clinique de Montchoisi

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-05-31
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 NCT01362868 on ClinicalTrials.gov