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NCT03085901 Clinical Trial

Comparison of Clinical Outcomes of Toric Intraocular Lens

Astigmatism Clinical Trial

Official title:
Comparison of Clinical Outcomes of Toric Intraocular Lens

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03085901
Other study ID # 2016-04-147
Secondary ID
Status Completed
Phase N/A
First received March 11, 2017
Last updated March 15, 2017
Start date April 2016
Est. completion date October 2016

Study information
Verified date March 2017
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to compare the clinical outcome of Precizon toric intraocular lens(IOL) to that of Tecnis toric IOL.

Description:

In cataract surgery, after phacoemulsification, intraocular lens should be implanted for patient's better visual acuity. When patient has large amount of corneal astigmatism, toric intraocular lens are recommended to correct the preexisting astigmatism.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date October 2016
Est. primary completion date July 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patient with cataract and regular corneal astigmatism(between 0.50 diopter and 2.50 diopter considering both anterior and posterior corneal surface)

Exclusion Criteria:

- Amblyopia, irregular astigmatism, corneal opacity, glaucoma, retinal disease, history of ocular inflammation, previous other intraocular surgery

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Precizon toric intraocular lens
Phacoemulsification and implantation of Precizon toric intraocular lens
• Tecnis toric intraocular lens
Phacoemulsification and implantation of Tecnis toric intraocular lens

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Samsung Medical Center

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative refractive astigmatism Diopter postoperative 3 months
Secondary Postoperative visual acuity logMAR postoperative 3 months
See also
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Completed NCT01211535 - Subjective Comfort With Multipurpose Care Solutions in Soft Contact Lens Wearers N/A