Rebound Esthesiometer Phase 2 Protocol

Trial Information
Status: Not yet recruiting
Intervention Type: Device
Study Type: Observational
Summary

The purpose of this study is to define the operating parameters for a new method to measure corneal sensitivity.

Am I eligible for this trial?
Participation Requirements
Sex:
All
Minimum Age:
18
Healthy Volunteers:
Accepts Healthy Volunteers

• Age >= 18

• Informed consent signed

Who do I contact about this trial?
Primary
Mika Salkola, M.Sc.
mika.salkola@icarefinland.com
+358400874054
Backup
Teemu Herranen, B.Sc.
teemu.herranen@icarefinland.com
+358415033680
When is this trial taking place?
Start Date: August 2020
Estimated Completion Date: December 2020
How many participants will be in this trial?
Target number of participants: 100
What treatment is being studied in this trial?
Test subjects
Test subjects according to the inclusion / exclusion criterias.
Who are the authors of this trial?
Matjaz Mihelcic
What other conditions are being studied in this trial?

This content was sourced from clinicaltrials.gov