Overview

Neural Compensation, Visual Function and Visual Quality After Monofocal or Multifocal Intraocular Lens Implantation

Status:
Unknown status
Trial end date:
2019-01-01
Target enrollment:
0
Participant gender:
All
Summary
Multifocal intraocular lenses (MIOLs) provide enhanced far and near visual acuity, but they can bring about halos and glare, which are caused by design deficiencies of the IOLs. Compared to monofocal intraocular lens, pseudo accommodation in nonphysiological state may increase the difficulty of neural compensation reconstruction in patients with multifocal intraocular lens implantation. Patients enrolled into the study will be followed for 1 year and will have study visits preoperatively, at 1 week, 3 months, 6 months, 12 months postoperatively.In this trial, we aimed to specify the time of neural compensation reconstruction in patients and to explore the changes of visual function in senile patients with monofocal or multifocal intraocular lens implantation.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sun Yat-sen University
Collaborator:
First Affiliated Hospital, Sun Yat-Sen University
Treatments:
BB 1101
Dexamethasone
Dexamethasone 21-phosphate
Dexamethasone acetate
Criteria
Inclusion Criteria:

- visual acuity less than 0.3

- Cataracts in both eyes classified by the Lens Opacity Classification System III

- Corneal astigmatism less than 1.5 diopters (D)

- Capability of understanding and signing the informed consent

Exclusion Criteria:

- Corneal astigmatism ≥ 1.5D.

- History of neurological or psychiatric disorders; systemic disease such as severe
hypertension or diabetes mellitus that might interfere with the visual outcomes.

- Associated ocular disease that could interfere with final results

- Previous anterior and posterior segment surgery and intraoperative or postoperative
complications

- Driving at night frequently; excessive expectations for visual outcomes