Assessment of an intraocular lens to provide independence from optical aids at all distances following cataract surgery in patients with astigmatism.

Not Applicable

Completed

• Conditions: Cataract; Eye - Diseases / disorders of the eye

• Registration Number: ACTRN12619001109190
• Lead Sponsor: Alcon Laboratories

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-08-12
• Study Completion: 2020-12-01
• Last Update Posted: 16 February 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

Subjects are eligible for the study if they meet the following criteria:
Note: Ocular criteria must be met in both eyes.
- are more than 40 years of age, of either gender and any race;
- have completed uncomplicated cataract surgery or refractive lens exchange surgery with the Alcon Panoptix Toric IOL at least 6 months prior (but no greater than 12 months)
- regular corneal astigmatism requiring toric IOL correction

Exclusion Criteria

If any of the following exclusion criteria are applicable to the subject or either eye, the subject should not be enrolled in the study.
- Amblyopia
- Previous anterior or posterior chamber surgery (e.g., vitrectomy, laser iridotomy)
- Diabetic retinopathy
- Macular degeneration
- History of retinal detachment
- Subjects who have an acute or chronic disease or illness that would confound the results of this investigation (e.g., immunocompromised, connective tissue disease, clinically significant atopic disease, diabetes, and any other such disease or illness), that are known to affect post-operative visual acuity.

Study & Design

• Study Type: Observational
• Study Design: Not specified