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Clinical Trials/NCT04706455
NCT04706455UnknownNot Applicable

Effect of Artificial Tears on the Parameters of the Eye in Normal and Dry Eyes and Its Impact on IOL Power Calculation for Cataract Surgery

Second Affiliated Hospital of Xi'an Jiaotong University1 site in 1 country60 target enrollmentStarted: December 1, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
keratometric value of the eye measured with Master 500 before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Study Overview

Brief Summary

First, preoperative biometry of the eye at the IOL Master® will be performed. Then, corneal topography will be measured at the Oculus pentacam®. Afterwards, one of two eye drops are instilled in the eye, and biometry and corneal topography will be repeated after 5 minutes.

For all patients, the Barrett Universal II formula will be used for calculation of IOL power. Predicted refraction outcome will be referred to as SEQ. The chief surgeon will perform the uneventful standard cataract operation with in-the-bag implantation of a HOYA IOL (Model 251) through a 2.4-mm corneal incision.

A Subjective Refraction using plus principle will be performed one month after the operation, and ETDRS visual acuity charts will be used to measure best-corrected visual acuity. Refraction will be described as SR (postoperative SEQ) and will be calculated as:

SR = sphere + (0.5*cylinder)

Detailed Description

First, preoperative biometry of the eye at the IOL Master® will be performed. Then, corneal topography will be measured at the Oculus pentacam®. Patients will be classified as dry eye or normal eye based on BUT. The tear film breakup (BUT) time of less than 5 seconds will be diagnosed as dry eyes.Afterwards, one of two eye drops are instilled in the eye, and biometry and corneal topography will be repeated after 5 minutes.

For all patients, the Barrett Universal II formula will be used for calculation of IOL power. Predicted refraction outcome will be referred to as SEQ. The chief surgeon will perform the uneventful standard cataract operation with in-the-bag implantation of a HOYA IOL (Model 251) through a 2.4-mm corneal incision.

A Subjective Refraction using plus principle will be performed one month after the operation, and ETDRS visual acuity charts will be used to measure best-corrected visual acuity. Refraction will be described as SR (postoperative SEQ) and will be calculated as:

SR = sphere + (0.5*cylinder)

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
30 Years to 95 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • A patient diagnosed with age related cataract
  • 30 to 95 years old
  • Medical history and physical examination should be normal.

Exclusion Criteria

  • • Abnormality of the cornea (scaring of the cornea)
  • If any topical therapy (i.e. glaucoma) of the eye is needed
  • Active allergy of eye or nose
  • Any conjunctivitis or keratitis
  • If nasolacrimal drainage apparatus is abnormal
  • severity level 4 of dry eye (constant discomfort in the eye accompanied with visual symptoms, filamentary keratitis, , keratinization, severe conjunctival injection, ulceration clumping of mucus glands, tear debris, , trichiasis, symblepharon)
  • deformities of lid
  • Preceding eye trauma or surgery
  • Any Uncontrolled ocular disease or systemic disease
  • Lactation
  • Pregnancy

Outcomes

Primary Outcomes

keratometric value of the eye measured with Master 500 before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Time Frame: 5 minutes

k-value (k, k1, k2 in Diopter)

Postoperative spherical equivalent (SE) measured one month after surgery.

Time Frame: one month after surgery

Postoperative spherical equivalent (SE in Diopters)

Sim K of the eye measured with Oculus Pentacam before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Time Frame: 5 minutes

Sim K (k1, k2 in Diopter)

Total Corneal Irregular Astigmatism of the eye measured with Oculus Pentacam before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Time Frame: 5 minutes

Total Corneal Irregular Astigmatism (TCIA in Diopter)

Predicted spherical equivalent (SE) calculated with Barrett Universal II formula before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Time Frame: 5 minutes

Predicted spherical equivalent (SEQ in Diopter)

Axial length of the eye measured with Master 500 before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Time Frame: 5 minutes

Axial length (AL in mm)

Anterior chamber depth of the eye measured with Master 500 before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Time Frame: 5 minutes

Anterior chamber depth (ACD in mm)

Total Corneal Refractive Power of the eye measured with Oculus Pentacam before and after 5 minutes of installation of artificial tears (sodium hyaluronate 0.1% or 0.3% eye drops).

Time Frame: 5 minutes

Total Corneal Refractive Power (TCRP in Diopter),

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Second Affiliated Hospital of Xi'an Jiaotong University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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