NCT01467453

Brief Summary

The study objective is to investigate the clinical applicability of continuous IOP measurement using TS with radio transmission over 24 hours.

  • Trial with medical device

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Nov 2011

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2011

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

November 3, 2011

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 8, 2011

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2012

Completed
Last Updated

November 16, 2011

Status Verified

November 1, 2011

First QC Date

November 3, 2011

Last Update Submit

November 14, 2011

Conditions

Glaucoma

Interventions

TriggerfishDEVICE

The Triggerfish is a contact lens with an embedded sensor to track changes in intraocular pressure during a period of 24 hours.

Also known as: Triggerfish, SENSIMED AG, Route de Chavannes 37, 1007 Lausanne, Switzerland

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients with a diagnosis of glaucoma

You may qualify if:

  • Clinical diagnosis of glaucoma

You may not qualify if:

  • Other opticus neuropathy than glaucoma
  • Corneal abnormalities (e.g. scaring)
  • Dry eye disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Zurich, Ophthalmic Clinic

Zurich, Switzerland

Location

MeSH Terms

Conditions

Glaucoma

Condition Hierarchy (Ancestors)

Ocular HypertensionEye Diseases

Study Officials

  • 01 Studienregister MasterAdmins

    UniversitaetsSpital Zuerich

    STUDY DIRECTOR

  • Christoph Kniestedt, Assistant Prof, MD

    University Hospital Zurich, Ophtalmic Clinic

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 3, 2011

First Posted

November 8, 2011

Study Start

November 1, 2011

Study Completion

December 1, 2012

Last Updated

November 16, 2011

Record last verified: 2011-11

Locations

CH(1)