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

Sponsor
Second Affiliated Hospital of Xi'an Jiaotong University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04706455
Collaborator
(none)
60
1
2
3
20.3

Study Details

Study Description

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)

Condition or Disease Intervention/Treatment Phase
  • Device: sodium hyaluronate 0.1%
  • Device: sodium hyaluronate 0.3%
N/A

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
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Corneal topography and Biometry will be performed in individuals with age-relate cataract. 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. One of two artificial tear eye drops will be instilled in the eye, and corneal topography and biometry will be repeated after 5 minutes of applicationCorneal topography and Biometry will be performed in individuals with age-relate cataract. 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. One of two artificial tear eye drops will be instilled in the eye, and corneal topography and biometry will be repeated after 5 minutes of application
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
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
Actual Study Start Date :
Dec 1, 2020
Anticipated Primary Completion Date :
Feb 1, 2021
Anticipated Study Completion Date :
Mar 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: sodium hyaluronate 0.1%

First preoperative Biometry of the eye at the IOL Master® will be measured. Then, corneal topography will be measure at the Oculus pentacam®. Afterwards, sodium hyaluronate 0.1% will be installed and biometry and corneal topography will be repeated after 5 minutes.

Device: sodium hyaluronate 0.1%
Instillation of one drop sodium hyaluronate 0.1%

Active Comparator: sodium hyaluronate 0.3%

First preoperative Biometry of the eye at the IOL Master® will be measured. Then,corneal topography will be measure at the Oculus pentacam®. Afterwards, sodium hyaluronate 0.3% will be installed and biometry and corneal topography will be repeated after 5 minutes.

Device: sodium hyaluronate 0.3%
Instillation of one drop sodium hyaluronate 0.3%

Outcome Measures

Primary Outcome Measures

  1. 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). [5 minutes]

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

  2. 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). [5 minutes]

    Axial length (AL in mm)

  3. 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). [5 minutes]

    Anterior chamber depth (ACD in mm)

  4. 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). [5 minutes]

    Sim K (k1, k2 in Diopter)

  5. 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). [5 minutes]

    Total Corneal Refractive Power (TCRP in Diopter),

  6. 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). [5 minutes]

    Total Corneal Irregular Astigmatism (TCIA in Diopter)

  7. 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). [5 minutes]

    Predicted spherical equivalent (SEQ in Diopter)

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

    Postoperative spherical equivalent (SE in Diopters)

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 95 Years
Sexes Eligible for Study:
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Ophthalmology, Second affiliated hospital of Xian Jiaotong University Xi'an Shaanxi China 710004

Sponsors and Collaborators

  • Second Affiliated Hospital of Xi'an Jiaotong University

Investigators

  • Principal Investigator: Ling Bai, MD,PhD, Second Affiliated Hospital of Xi'an Jiaotong University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Second Affiliated Hospital of Xi'an Jiaotong University
ClinicalTrials.gov Identifier:
NCT04706455
Other Study ID Numbers:
  • 20210312
First Posted:
Jan 12, 2021
Last Update Posted:
Jan 12, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 12, 2021