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Clinical Trials/NCT02362334
NCT02362334
Unknown
Not Applicable

Precision of Optical Biometry and Intraocular Lens Power Calculation Using Dual Schiempflug Analyzer

Chuncheon Sacred Heart Hospital1 site in 1 country140 target enrollmentOctober 2014
ConditionsCataract

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataract
Sponsor
Chuncheon Sacred Heart Hospital
Enrollment
140
Locations
1
Primary Endpoint
Ocular parameters
Last Updated
11 years ago

Overview

Brief Summary

This study evaluates the various ocular parameters which are necessary for ocular biometry and the calculated IOL powers using both dual Schiempflug analyzer and optical low-coherence refelctometry.

Detailed Description

The measured keratometry, axial length, anterior chamber depth, lens thickness, white-to-white corneal diameter, and calculated IOL powers using various formulas including Hoffer Q, Holladay I, SRK II and SRK T measured by dual Schiempflug analyzer and optical low-coherence refelctometry will be compared.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
February 2015
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Chuncheon Sacred Heart Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • axial length between 21.0 and 27.0 mm
  • older than 20 years old

Exclusion Criteria

  • other ophthalmic diseases such as severe dry eye, glaucoma, and age-related macular degeneration
  • previous ophthalmic surgery including cataract surgery, and refractive surgery
  • very dense media which cannot be measured by the optical biometries
  • severe zonulysis

Outcomes

Primary Outcomes

Ocular parameters

Time Frame: Single point

Parameters measured using two devices were compared at a single point

Calculated IOL powers

Time Frame: Single point

Calculated IOL powers using two devices were compared at a single point

Study Sites (1)

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