Clinical Evaluation of HPT Treated Rigid Contact Lenses Made From

Clinical Trial Summary

This will be an up to six months, subject-masked, contralateral, parallel-group, randomised, daily wear study. All subjects will wear the Test lens in one eye and the Control lens in the other eye. Data from the first four weeks of Test and Control lens exposure will be used for the FDA 510 (k) submission.

See also
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Recruiting	`NCT04632784` - Clinical Trial With Artiflex Presbyopic	N/A
Completed	`NCT04185701` - Comparison of Subjective Refraction Measurement With SiVIEW Software and by an Expert	N/A
Completed	`NCT01706770` - Evaluation of Enfilcon A Soft Contact Lens When Compared to Galyfilcon A Soft Contact Lens	N/A
Completed	`NCT03556579` - The Effects of Contact Lenses With Experimental Dye on Visual Function	N/A
Completed	`NCT04654455` - Prospective Study Evaluating Dry Eye in Patients Operated on for Ametropia by LASIK Surgery and Treated With REPADROP
Not yet recruiting	`NCT06295536` - Optimization of a Photoretinoscopy Method for Determining the Objective Refraction of Children	N/A
Completed	`NCT00691197` - Safety and Acceptability of Using a Rewetting Drop With Contact Lens Wear	Phase 2/Phase 3
Completed	`NCT00597467` - Study of Soft Contact Lens Use With 7 Day Extended Wear	N/A
Completed	`NCT04067141` - The Clinical Comparison of Somofilcon A 1 Day and Nelfilcon A Daily Disposable Contact Lenses	N/A
Completed	`NCT04067050` - A Clinical Study of the Comfilcon A Asphere Soft Contact Lens in Users of Digital Devices	N/A
Completed	`NCT00722891` - Ocular Responses to Short and Long-term Lens Wear	N/A
Completed	`NCT00349063` - Contact Lens Wettability	Phase 4

NCT number	NCT02553681
Study type	Interventional
Source	Contamac Ltd
Contact
Status	Completed
Phase	N/A
Start date	July 2015
Completion date	February 16, 2017

Clinical Evaluation of HPT Treated Rigid Contact Lenses Made From Roflufocon D

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms