Skip to content

Functional and Physiological Changes Induced by Pinhole Glasses in Presbyopia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02722291
Enrollment
40
Registered
2016-03-30
Start date
2016-03-31
Completion date
2017-03-31
Last updated
2016-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pinhole

Keywords

presbyopia

Brief 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.

Interventions

Sponsors

Chung-Ang University Hosptial, Chung-Ang University College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Distant visual acuity (logMAR)Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyDistant visual acuity were measured using Snellen chart (Precision Vision, La Salle, IL, USA) at 4 m.
BUTSubjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyfluorescein 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
Near point of accommodation (NPA)Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyNear point of accommodation (NPA) was measured using Donder's push-up method.
The fusional convergenceSubjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyWith 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.
StereopsisSubjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyStereopsis was checked with the Randot Stereotest (Stereo Optical Co., Chicago, IL, USA).
Reading speed (letters per second)Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyReading speed was evaluated using the famous Korean traditional fairy tale book. This Korean book was printed black-and-white with 10-font size.
Photopic pupil size (baseline, mm)Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyPupil size under photopic conditions (85 cd/m2) was measured using a WASCA Analyzer (Carl Zeiss Meditec, Oberkochen, Germany).
Pupil size with the one eye pinhole glasses (mm)Subjects performed this examination while wearing multiple pinhole and without wearing pinhole with one week apart in random order after baseline studyPupil size with the one eye pinhole glasses was measured using a WASCA Analyzer (Carl Zeiss Meditec, Oberkochen, Germany).

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026