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RECRUITINGINTERVENTIONAL

Refractive Outcomes and Ocular Biometry of Two Swept-Source Optical Coherence Tomography-Based Biometers With Segmental or Equivalent Refractive Indices (ORION)

Refractive Outcomes and Ocular Biometry of Two Swept-Source Optical Coherence Tomography-Based Biometers With Segmental or Equivalent Refractive Indices (ORION): A Non-Inferiority Randomized Clinical Trials

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Cataract surgery represents a common surgical intervention, encompassing the extraction of the opaque natural crystalline lens, followed by the substitution with an artificial intraocular lens (IOL). To ascertain an IOL possessing optimal power, antecedent to the surgery, preoperative evaluations are conducted through the utilization of a biometric devices. Diverse categories of these instruments are accessible, each harnessing distinct optical methodologies or mathematical algorithms to ascertain the most fitting IOL power. The principal objective of this study was to evaluate the ocular biometry and the predictive precision outcome of a biometer that uses standard keratometry to the prediction accuracy of another biometer that uses Total Keratometry.

Who May Be Eligible (Plain English)

Who May Qualify: • Patients with cataract and/or presbyopia who will undergo intraocular lens implantation. Who Should NOT Join This Trial: - Central corneal thickness less than 490 mm or greater than 600 mm - Contact lens use within 2 months of cataract surgery - Severe dry eye - Corneal or retinal disease affecting visual outcome - Corneal astigmatism greater than 1.00 D - Prior corneal refractive surgery - Dense cataract that does not allow measurements to be taken with an optical biometrics system. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: • Patients with cataract and/or presbyopia who will undergo intraocular lens implantation. Exclusion Criteria: * Central corneal thickness less than 490 mm or greater than 600 mm * Contact lens use within 2 months of cataract surgery * Severe dry eye * Corneal or retinal disease affecting visual outcome * Corneal astigmatism greater than 1.00 D * Prior corneal refractive surgery * Dense cataract that does not allow measurements to be taken with an optical biometrics system.

Treatments Being Tested

DEVICE

IOLMaster 700 (Carl Zeiss Meditec AG)

Subjects will undergo measurements with the IOLMaster 700 device.

DEVICE

Argos (Alcon Laboratories, Inc.)

Subjects will undergo measurements with the Argos device.

Locations (1)

Walailak University
Nakhon Si Thammarat, Thailand