Cataract
Conditions
Interventions
Group A:TECNIS Symfony EDOF intraocular lens and TECNIS monofocal intraocular lens(ZCB00)
Group B:AT LISA tri 839MP intraocular lens or AcrySof IQ PanOptix intraocular lens and Zeiss monofocal intraocular lens(409) or AcrySof monofocal intraocular lens(IQ)
Sponsors
Eye & ENT Hospital of Fudan University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Aged >=18 years; 2. The operated eye has ever undergone corneal refractive surgery, including PRK, LASIK, LASEK, FS-LASIK, SMILE and excluding RK; 3. At least one eye suffering from cataract and expected to undergo phacoemulsification and IOL implantation and cataract nuclei rigidity in the operated eye from 1 to 3 degree; 4. Expected to use intraocular lens power in -10.0D~+30.0D; 5. Willing and able to comply with scheduled visits and other study procedures; 6. The need to decrease the dependence of glasses; 7. Signing an informed consent form.
Exclusion criteria
Exclusion criteria: 1. Any vision-limiting problems (e.g., corneal, retinal, infection) which could potentially limit their post-operative visual potential; 2. Any newly acquired ocular condition or pathology (e.g., ARMD, epiretinal membrane, chronic dry eye, irregular astigmatism, diabetic retinopathy); 3. The density of corneal endothelial cells is lower than 2000/mm2; 4. The natural diameter of the pupil under the darkroom is less than 3mm or greater than 5.5mm; 5. The Kappa or Alpha angle of the operated eye is greater than 0.5mm, or the Kappa angle is greater than half of the diameter of the central refractive optical zone in the multifocal intraocular lens; 6. Patients with expected best corrected distance visual acuity(BCDVA) less than 0.5 (decimal vision); 7. Occurrence of irregular corneal astigmatism that affects postoperative vision; 8. Intraocular conventional surgery within the past three months or intraocular laser surgery within one month in the operated eye; 9. Pregnant, lactation or planning to become pregnant in the near future; 10. Any surgical contraindications; 11. Uncontrolled systemic or ocular disease; 12. Use of any systemic or topical drug known to interfere with visual performance; 13. Other ocular surgery at the time of the cataract extraction; 14. Traumatic cataract or congenital bilateral cataract in the operated eye; 15. Getting used to reading with glasses; 16. High requirements for visual functions in patients' career or daily life; 17. Professional drivers or frequent outdoor workers at night; 18. A medical history of photophobia; 19. Amblyopia; 20. Excessive vision expectations after surgery or too sensitive, nervous, depressed or picky; 21. Unsupervised or unable to comply with scheduled visits; 22. The contralateral eye was judged to lose visual function; 23. Other situations where the researcher judges that the patient is not suitable for inclusion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative UDVA measured with standard visual acuity charts;Postoperative UIVA measured with standard visual acuity charts;Postoperative UNVA measured with standard visual acuity charts;the rate of taking glasses off;Defocus Curve;Postoperative satisfaction; | — |
Secondary
| Measure | Time frame |
|---|---|
| monocular visual acuity;Diopter;IOL rotation stability;wavefront aberration;contrast sensitivity;Binocular vision; | — |
Countries
China
Contacts
Public ContactYinghong Ji
Eye & ENT Hospital of Fudan University
Outcome results
None listed