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Clinical Trials/NCT05564455
NCT05564455CompletedNot Applicable

Comparison of SRK-T With Kane Formula for Prediction of Refractive Outcome After Phacoemulsification

Foundation University Islamabad1 site in 1 country70 target enrollmentStarted: June 17, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
70
Locations
1
Primary Endpoint
Post-operative refractive outcome in diopters

Study Overview

Brief Summary

Cataract is a leading cause of blindness in the world. Cataract surgery is one of the most commonly performed ocular procedures. We aim to compare the newer generation biometry formula; the Kane formula with the commonly used SRK-T formula for intraocular power calculation in uneventful phacoemulsification surgery to assess the post-operative refractive outcomes at one month post-surgery.

Detailed Description

Purpose: To compare post-operative refractive outcome with Sanders Retzlaff Kraff theoretical (SRK T) and Kane formulae for intraocular lens (IOL) power calculation in cataract patients Study Design: Prospective, interventional study Place and Duration of Study: Department of Ophthalmology, Fauji Foundation Hospital, Rawalpindi Material and Methods: A total of a 70 eyes, 35 in each group will be included in our study. The patients will be randomly divided into two groups. In cases of bilateral cataract, one eye will be included in each group for better control. IOL power calculation in Group A will be done with the SRK-T formula and in group 2 with the Kane Formula. Autokeratometry and A-scan ultrasound will be done for biometry. Inclusion criteria will be uncomplicated cataract in both genders. Exclusion criteria will be ocular trauma, uveitis, previous intraocular surgery, or any retinopathy. All patients will undergo phacoemulsification with foldable lens implantation by two experienced surgeons. Post-operative refractive outcome will be evaluated at one month after surgery. The two groups will be compared.

Results: The results will be calculated by SPSS. Conclusion: A conclusion will be drawn on the basis of our results.

Study Design

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

Eligibility Criteria

Ages
40 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Senile cataract (nuclear, cortical, posterior subcapsular, mature, hypermature cataract)
  • Absence of other ocular pathology causing diminished visual acuity
  • patients above 40 years of age
  • Astigmatism > 2.5 diopters

Exclusion Criteria

  • Retinal diseases
  • Maculopathy
  • Complications during phacoemulsification
  • Combined procedures
  • Previous ocular surgery
  • Secondary cataract

Outcomes

Primary Outcomes

Post-operative refractive outcome in diopters

Time Frame: 1 hour to 1 year

Post-operative refractive outcome will be compared with intended refractive outcome

Visual acuity (Snellen/logMAR) and refractive error (automated refraction in diopters)

Time Frame: 1 month post-operatively

The visual acuity and refractive error of the patients will be measured 1 month post-operatively to compare between the two groups

Spherical equivalent in diopters

Time Frame: 1 hour to 1 year

The spherical equivalent of the patients will be measured 1 month post-operatively to compare between the two groups

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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