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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02939001
Other study ID # 1-2016-0049
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 3, 2016
Est. completion date March 24, 2017

Study information

Verified date July 2018
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study included patients who visit for refractive surgery (photorefractive keratectomy, photorefractive keratectomy with with corneal collagen cross linking, laser in situ keratomileusis, small incision lenticule extraction), phakic Intraocular Lens implantation (Implantable Collamer Lens, artiflex), and cataract surgery. Patients will be examined whether iris recognition scanner of smartphone works before and after surgery. In addition, before and after pupil dilation (5mm, 6mm, 7mm, 8mm), patients will be examined whether iris recognition scanner of smartphone works well.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date March 24, 2017
Est. primary completion date March 24, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 90 Years
Eligibility Inclusion Criteria:

- Patients who visit for refractive surgery (photorefractive keratectomy, photorefractive keratectomy with with corneal collagen cross linking, laser in situ keratomileusis, small incision lenticule extraction)

- phakic Intraocular Lens implantation (Implantable Collamer Lens, artiflex)

- cataract surgery.

- age of 20~90

Exclusion Criteria:

- history of previous ocular or intraocular surgery

- glaucoma or ocular hypertension, ocular infection, non-dry eye ocular inflammation, ocular allergy, autoimmune disease

- history of iris damage during ocular surgery or previous trauma

- wearing contact lenses during the study period

- presence of current punctal occlusion

- pregnancy, lactating women, and children

Study Design


Related Conditions & MeSH terms


Intervention

Device:
iris recognition scanner


Locations

Country Name City State
Korea, Republic of Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary capability of iris recognition scanner Patients will be examined whether iris recognition scanner of smartphone works 1 day before refractive surgery (photorefractive keratectomy, photorefractive keratectomy with corneal collagen cross linking, laser in situ keratomileusis, small incision lenticule extraction), phakic Intraocular Lens implantation (Implantable Collamer Lens, artiflex), and cataract surgery. 1 day before the surgery
Primary capability of iris recognition scanner Patients will be examined whether iris recognition scanner of smartphone works 1 week after refractive surgery (photorefractive keratectomy, photorefractive keratectomy with corneal collagen cross linking, laser in situ keratomileusis, small incision lenticule extraction), phakic Intraocular Lens implantation (Implantable Collamer Lens, artiflex), and cataract surgery. 1 week after the surgery
Secondary pupil dilation Patients will be examined whether iris recognition scanner of smartphone works well 1 day before pupil dilation. 1 day before pupil dilation
Secondary pupil dilation Patients will be examined whether iris recognition scanner of smartphone works well 1 week after before pupil dilation. 1 week after the surgery
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