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Refractive Outcomes and Ocular Biometry of Two Swept-Source Optical Coherence Tomography-Based Biometers With Segmental or Equivalent Refractive Indices (ORION) - Trial NCT06377007

Access comprehensive clinical trial information for NCT06377007 through Pure Global AI's free database. This phase not specified trial is sponsored by Walailak University and is currently Recruiting. The study focuses on Cataract. Target enrollment is 142 participants.

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ClinicalTrials.gov โ€ข NCT06377007
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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

Study Focus

Cataract

IOLMaster 700 (Carl Zeiss Meditec AG)

Interventional

device

Sponsor & Location

Walailak University

Nakhon Si Thammarat, Thailand

Timeline & Enrollment

N/A

Jan 01, 2024

Dec 30, 2025

142 participants

Primary Outcome

Mean absolute prediction error

Summary

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.

ICD-10 Classifications

Other cataract
Cataract, unspecified
Complicated cataract
Other specified cataract
Senile cataract

Data Source

ClinicalTrials.gov

NCT06377007

Device Trial