Evaluation of Safety and Performance of the EyenableTM Intraocular Lens for Cataract Treatment
Launched by XI'AN EYEDEAL MEDICAL TECHNOLOGY CO., LTD · Jan 16, 2024
Trial Information
Current as of October 09, 2024
Not yet recruiting
Keywords
Description
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- 1. Adults (≥ 18 years of age at the time of surgery) of any gender, diagnosed with age related cataracts in one or both eyes.
- 2. Opacity of crystalline lens due to cataract and reduced vision assessed by patient complaints.
- 3. Calculated lens power within the available range for the EyenableTM PA60AS1 IOL (+10D to +30.00D)
- 4. Planned cataract removal by phacoemulsification procedure
- 5. Clear intraocular media other than cataract, in the study eye
- 6. Pharmacologically dilated pupil size of at least 6.0mm.
- 7. 2.0 D or less of preoperative astigmatism in the study eye
- 8. Willing and able to complete all required postoperative visits
- 9. Able and willing to comprehend and sign or through a representative, with a witness present, an EC approved Informed Consent Form (ICF).
- Exclusion Criteria:
- 1. Subject who, in the judgment of the clinical investigator, is not suitable for participation in the study for any clinical reason, as documented by the investigator on the patient's Case Report Forms (CRFs).
- 2. Any type of cataract other than age-related.
- 3. History of any intraocular, retinal, corneal or refractive surgery in the study eye (including LASIK, PRK, SMILE, etc.), only in the opinion of investigator that it could confound study outcome
- 4. Ocular conditions which could affect the stability of the IOL (e.g., pseudoexfoliation, zonular dialysis, evident zonular weakness or dehiscence, etc.) in the study eye.
- 5. Any anterior segment pathology likely to increase the risk of complications from phacoemulsification cataract extraction (e.g., chronic uveitis, iritis, iridocyclitis, aniridia, rubeosis iridis, clinically significant corneal disorders, (Fuchs', or anterior basement membrane dystrophy, etc.) in the study eye.
- 6. Mature cataract that is likely to prolong phacoemulsification and/or lead to intraoperative complications prior to attempted IOL implantation.
- 7. Any visually significant intraocular media opacity other than cataract in the study eye.
- 8. History of any clinically significant retinal pathology or ocular diagnosis (e.g., diabetic retinopathy, ischemic disease, macular degeneration, retinal detachment, amblyopia, optic neuropathy, microphthalmos, aniridia, neuro-ophthalmic disease, fixation problems etc.) in the study eye that could alter or limit final postoperative visual prognosis.
- 9. History of cystoid macular edema in the study eye.
- 10. Severe dry eye that, in the opinion of the investigator, would impair the ability to obtain reliable study measurements.
- 11. Uncontrolled glaucoma and/or optic atrophy in the study eye.
- 12. Extremely shallow anterior chamber (\< 2.0 mm).
- 13. Irregular astigmatism, corneal degeneration or dystrophy.
- 14. Uncontrolled systemic disease (e.g., diabetes mellitus, active cancer treatment, mental illness, etc.) in the opinion of the investigator, would put the subject's health at risk and/or prevent the subject from completing all study visits.
- 15. Systemic medication that, in the opinion of the investigator, may confound the outcome or increase the intraoperative and post-operative risk to the subject (e.g., tamsulosin hydrochloride)
- 16. Subjects who may reasonably be expected to require any additional ophthalmic surgical intervention at any time during the study (other than YAG capsulotomy).
- 17. Need for concomitant procedures (e.g., glaucoma surgery, LRI, PRK, LASIK, etc.).
- 18. Participation in any other drug or device clinical trial within 30 days prior to enrolling this study and/or during study participation.
- 19. Pregnancy or lactation.
About Xi'an Eyedeal Medical Technology Co., Ltd
Xi'an Eyedeal Medical Technology Co., Ltd. is a leading innovator in the field of medical technology, specializing in the development and commercialization of advanced diagnostic and therapeutic solutions. With a strong commitment to enhancing healthcare outcomes, the company focuses on leveraging cutting-edge research and development to create products that meet the evolving needs of healthcare professionals and patients. Xi'an Eyedeal is dedicated to ensuring the highest standards of quality and efficacy in its clinical trials, fostering partnerships with clinical research organizations, and adhering to regulatory guidelines to drive advancements in medical technology.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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