Evaluating the Efficacy and Safety of Contact Lens Lubricant in Rigid Gas Permeable Corneal Contact Lens Wearers

Avizor SA

Status: Enrolling

Conditions: Myopia

Treatments: Device: LACRIFRESH OCU-DRY 0.3% OSD; Device: Rigid contact lens lubricant

Study type: Interventional

Funder types: Industry

Identifiers

NCT07091825

Avizor-CT

Details and patient eligibility

About

This trial aims to evaluate the safety and effectiveness of LACRIFRESH OCU-DRY 0.3% OSD, a contact lens lubricant produced by AVIZOR, S.A. This clinical trial adopts a Multi-center, randomized, open-label, positive parallel-controlled design in accordance with the principles outlined in the Norms on the Quality Management for the Clinical Trials of Medical Devices issued by the National Medical Products Administration of China.

Meanwhile, following statistical requirements, 152 rigid contact lens wearers are planned to be enrolled after screening and meeting the inclusion criteria. Participants will be randomly assigned to groups and provided with lenses, lubricants, and care solutions accordingly. Clinical follow-up assessments are scheduled at 1 week, 1 month, and 3 months after use.

The primary efficacy indexes are the percentage of patients with binocular comfort score ≥ Level 3 at the 1-month follow-up and the percentage of patients with best corrected distance visual acuity with contact lenses for both eyes ≥5.0 at the 1-month follow-up after using the contact lens lubricant. Secondary efficacy indexes include, best corrected distance visual acuity with lenses, visual acuity with lenses, residual diopter, tear break-up time, uncorrected visual acuity, examination of contact lens fitting status, lens assessment, and contact lens lubricant evaluation during the corresponding follow-up periods. Safety indexes include slit lamp examination, fundus examination, IOP, corneal endothelial cell, adverse events, serious adverse events, device defects that may lead to serious adverse events, other device defects during the corresponding follow-up periods.

Enrollment: 152 estimated patients

Sex: All

Ages: 8+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Aged 8 and older, no gender limitation;
2. Rigid gas permeable corneal contact lens (OK lens) wearers;
3. The best corrected distance visual acuity of framed lenses in both eyes can reach 5.0 (5-Point Scale);
4. Be able and willing to comply with all treatments and follow-ups;
5. Be able to understand the purpose of the trial, participate voluntarily and have ICF signed by the subject himself/herself or his/her legal guardian.

Exclusion criteria

1. Patients with only one eye meeting the inclusion criteria.
2. Patients with abnormal clinical abnormalities or systemic diseases affecting the eyes that occurred or is occurring before screening and, in the investigator's judgment, preclude the use of corneal contact lenses.
3. Patients with some eye diseases that affect contact lens wearing: such as acute or chronic eye diseases, conjunctivitis catarrhalis aestiva, glaucoma, corneal abnormalities, keratoconus, etc.
4. Patients with allergies to the components of contact lens or contact lens care solution involved in this trial;
5. Patients who are using or need to use drugs that may cause dry eyes or affect vision and corneal curvature (e.g. immunosuppressant, glucocorticoids, IOP-lowering drugs, low concentration atropine) during the study;
6. Patients with a history of intraocular operation;
7. Patients with abnormal IOP (the single eye IOP <10 mmHg or >21mmHg, or the IOP difference of both eyes >5mmHg), obvious fundus abnormalities, examination of corneal endothelial cell (abnormal ≥ Level 4), or slit-lamp examination abnormalities.
8. Patients with dry eye syndrome or with break up time (BUT) <5s.
9. Subjects who participated in other drug clinical trials within 90 days before screening, and participated in other medical device clinical trials within 30 days;
10. Patients who wore rigid contact lens (including orthokeratology lens) within the past 30 days;
11. Patients who are pregnant, nursing or planning to conceive at the enrollment;
12. Patients with contraindications for wearing rigid contact lenses or unsuitable for wearing rigid contact lenses as indicated by examination results;
13. Other conditions for which the investigator judged the patient unsuitable for inclusion.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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152 participants in 2 patient groups

Tested medical device

Experimental group

Description:

LACRIFRESH OCU-DRY 0.3% OSD

Treatment:

Device: LACRIFRESH OCU-DRY 0.3% OSD

Control medical device

Active Comparator group

Description:

Rigid contact lens lubricant

Treatment:

Device: Rigid contact lens lubricant