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Clinical Trials/NCT04952181
NCT04952181
Unknown
Not Applicable

Optical Biometry Versus Ultrasonic Biometry in Intraocular Lens Calculation in High Myopic Cataractous Patients: A Comparative Study

Sohag University0 sites40 target enrollmentJuly 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Calculation of Intraocular Lens in High Myopic Cataractous Patients
Sponsor
Sohag University
Enrollment
40
Primary Endpoint
desired post operative refraction
Last Updated
4 years ago

Overview

Brief Summary

the purpose of the study is to compare the accuracy of optical and ultrasonic biometry in intraocular lens (IOL) calculation in high myopic cataractous patients

Detailed Description

* Prospective interventional (QUASI experimental) comparative study * This study will be conducted on high myopic cataractous patients scheduled for phacoemulsification and IOL implantation in department of ophthalmology, Sohag university * patients will be divided into 2 groups one will be subjected to intraocular lens (IOL) calculation by optical biometry the second one will be subjected to intraocular lens (IOL) calculation by ultrasonic biometry * postoperative auto refraction after I month

Registry
clinicaltrials.gov
Start Date
July 2021
End Date
February 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Esraa Ahmed Okasha

principle investigator

Sohag University

Eligibility Criteria

Inclusion Criteria

  • patients with simple cataract not associated with other pathologies suitable for phacoemulsification and 1ry IOL implantation With axial length (AXL) equal to or greater than 26.5mm

Exclusion Criteria

  • History of trauma
  • Associated pathologies such as optic neuropathy, age related macular degeneration, macular edema, retinal detachment, , ocular inflammation, retinitis pigmentosa, proliferative diabetic retinopathy
  • corneal opacities or irregularities, scars, dystrophy or ectasia
  • Patients who underwent previous corneal surgery (including refractive surgery)
  • Patients having intraoperative complications as inability to achieve secure 'in the bag' placement of the IOL (i.e. due to posterior capsule rupture, vitreous loss, weak zonules, or zonular rupture)

Outcomes

Primary Outcomes

desired post operative refraction

Time Frame: postoperative refraction 1 month

detection of postoperative refraction by the use of autorefractor (one of the objective methods of assessment of refraction) after use of IOL power calculated by different investigations (optical vs ultrasonic)

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