Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02722291
Other study ID # ChungAngUHophthalmology
Secondary ID
Status Recruiting
Phase N/A
First received March 21, 2016
Last updated March 23, 2016
Start date March 2016
Est. completion date March 2017

Study information

Verified date March 2016
Source Chung-Ang University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study is aimed at presbyopic patients that do not require magnifying glass at close rage. The purpose of this study is to investigate the functional and physiological changes in eye induced by pinhole glass.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date March 2017
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 45 Years and older
Eligibility Inclusion Criteria:

1. age over 45 years

2. spherical equivalents(SE) within ± 3.0 diopters(D)

3. normal ocular alignment

Exclusion Criteria:

1. disturbance of accommodation due to any reasons such as an Adie's pupil, Parkinson's disease, a history of previous ocular surgery or trauma, and a history of systemic or topical medication that might affect accommodation

2. corneal pathologic features

3. glaucoma

4. cataracts of grade II or greater by the Lens Opacities Classification System III (LOCS III)

5. vitreous and retinal abnormalities that might limit the accuracy of testing

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Device:
Trayner Pinhole Glasses (Trayner Glasses, Ivybridge Devon, U.K.)


Locations

Country Name City State
Korea, Republic of Chung-Ang University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Chung-Ang University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Distant visual acuity (logMAR) Distant visual acuity were measured using Snellen chart (Precision Vision, La Salle, IL, USA) at 4 m. Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
Primary BUT fluorescein is instilled into the subject's tear film and the subject is asked not to blink while the tear film is observed under a broad beam of cobalt blue illumination Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
Primary Near point of accommodation (NPA) Near point of accommodation (NPA) was measured using Donder's push-up method. Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
Primary The fusional convergence With the subject watching the 20/30 sized fixation target at 40 cm, we take the base-out bar prism on the subject's right eye. While gradually increasing the extent of the prism, the first point that the subject noticed diplopia was defined as the break point. Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
Primary Stereopsis Stereopsis was checked with the Randot Stereotest (Stereo Optical Co., Chicago, IL, USA). Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
Primary Reading speed (letters per second) Reading speed was evaluated using the famous Korean traditional fairy tale book. This Korean book was printed black-and-white with 10-font size. Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
Primary Photopic pupil size (baseline, mm) Pupil size under photopic conditions (85 cd/m2) was measured using a WASCA Analyzer (Carl Zeiss Meditec, Oberkochen, Germany). Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
Primary Pupil size with the one eye pinhole glasses (mm) Pupil size with the one eye pinhole glasses was measured using a WASCA Analyzer (Carl Zeiss Meditec, Oberkochen, Germany). Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline study No
See also
  Status Clinical Trial Phase
Completed NCT05326607 - Pilot Clinical Investigation of Adaptative Eyeglasses for the Correction of Presbyopia N/A
Recruiting NCT06060041 - IC-8 Apthera IOL New Enrollment Post Approval Study
Completed NCT05495971 - Extended Depth of Focus Contact Lenses for Presbyopia N/A
Completed NCT05464732 - Vivity IOL: Emmetropia Compared to Monovision. N/A
Recruiting NCT06045299 - Evaluation of the Efficacy and Safety of LNZ101 and LNZ100 for the Presbyopia Phase 3
Active, not recruiting NCT04151550 - Safety & Efficacy of the Laser Scleral Microporation Procedure (Philippines) N/A
Not yet recruiting NCT05506553 - Comparison of Aspheric Toric Intraocular Lenses for Micro-monovision N/A
Completed NCT02554396 - Evaluation of the Efficacy and Safety of PRX-100 in the Treatment of Early to Moderate Presbyopia Phase 2
Completed NCT02235831 - DAILIES® AquaComfort Plus® Multifocal (MF) - Comparative Assessment of Visual Performance N/A
Completed NCT02214797 - Dispensing Study to Assess Visual Performance of Prototype Contact Lenses N/A
Enrolling by invitation NCT01443585 - Clinical Evaluation of a Progressive Addition Lens (PAL) N/A
Completed NCT01591499 - Clinical Evaluation of Biofinity Multifocal Compared With Air Optix Aqua Multifocal and With PureVision Multifocal N/A
Completed NCT04983589 - A Study to Assess Safety and Efficacy in Participants Age 40 to 55 With Presbyopia (Old Eye) Who Receive AGN-190584 in Both Eyes Twice Daily Phase 3
Completed NCT02740010 - The Visual Performances of a Progressive Multifocal Intraocular Lens With Extended Depth of Focus
Recruiting NCT05796453 - Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptix N/A
Completed NCT02516306 - A Study to Evaluate the Safety and Efficacy of EV06 Ophthalmic Solution in Improving Vision in Subjects With Presbyopia Phase 1/Phase 2
Completed NCT05359380 - The Impact of Light Conditions on the Efficacy of Multifocal Intraocular Lens Implantation in Activities of Daily Living
Not yet recruiting NCT04522427 - Study of Presbyopia-correcting Intraocular Lenses in Eyes With Previous Corneal Refractive Surgery N/A
Completed NCT03688425 - Comparison of Clinical Outcomes POD L GF vs POD F GF in Asian Eyes N/A
Recruiting NCT06053463 - Evaluation of Soft Multifocal Lenses in Presbyopic Previous Contact Lens Wearers N/A