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Use of an Ocular Telemetry Sensor in Diamox Treated Patients

NCT01028664 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2010-12-03

No results posted yet for this study

Summary

A soft contact lens integrating a Sensor is placed on subjects with high intraocular pressure (IOP) after administration of an IOP-lowering drug to investigate the device's capacity to detect the induced IOP reduction.

Conditions

Interventions

DEVICE

SENSIMED Triggerfish

2-hour continuous IOP monitoring

Sponsors & Collaborators

  • Clinique de Montchoisi, Lausanne, Switzerland

    collaborator UNKNOWN

  • Sensimed AG

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2010-10-31
Completion
2010-10-31

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

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 NCT01028664 on ClinicalTrials.gov