💬In plain words
What the trial is, and whether it could suit you
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
Sign in to get the eligibility rules as simple questions to take to your doctor.
📋 Eligibility rules (as published)
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.
💊
What it tests
- LACRIFRESH OCU-DRY 0.3% OSD
- Rigid contact lens lubricant
Beijing Aier Intech Eye Hospital
Beijing, China
Tianjin Eye Hospital
Tianjin, China
Tianjin Medical University Eye Hospital
Tianjin, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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