NCT02939001

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 3, 2016

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

October 18, 2016

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 19, 2016

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 24, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 24, 2017

Completed
Last Updated

July 18, 2018

Status Verified

July 1, 2018

Enrollment Period

6 months

First QC Date

October 18, 2016

Last Update Submit

July 15, 2018

Conditions

Outcome Measures

Primary Outcomes (2)

  • 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

  • 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 Outcomes (2)

  • pupil dilation

    1 day before pupil dilation

  • pupil dilation

    1 week after the surgery

Study Arms (1)

Ophthalmic surgery group

EXPERIMENTAL

Ophthalmic surgery group (refractive surgery, phakic Intraocular Lens implantation, and cataract surgery)

Device: iris recognition scanner

Interventions

Also known as: Galaxy Note 7 (Smartphone)
Ophthalmic surgery group

Eligibility Criteria

Age20 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine

Seoul, 03722, South Korea

Location

MeSH Terms

Conditions

CataractMyopiaAstigmatism

Condition Hierarchy (Ancestors)

Lens DiseasesEye DiseasesRefractive Errors

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 18, 2016

First Posted

October 19, 2016

Study Start

October 3, 2016

Primary Completion

March 24, 2017

Study Completion

March 24, 2017

Last Updated

July 18, 2018

Record last verified: 2018-07

Data Sharing

IPD Sharing
Will not share

Locations