Visual acuity was measured with the participant's habitual correction. All participants had a best corrected visual acuity of 20/25 or better. Non-cycloplegic autorefraction was measured for both eyes (WAM-5000; Grand Seiko, Tokyo, Japan). Axial length and central corneal thickness were measured using a non-contact low-coherence optical biometer (LenStar; Haag-Streit, Köniz, Switzerland). Five measurements were collected and averaged for each eye. Exclusion criteria included any ocular pathology, use of prescription or over-the-counter medications known to affect sleep or circadian rhythms, use of sleep aids such as melatonin, and shift work or travel across more than two time zones during the month prior to the study visit. No participants had any systemic disease with ocular manifestations, such as diabetes or hypertension.
Lenstar
The Lenstar is an optical biometry device designed for use in ophthalmology. It provides measurements of various ocular parameters, including corneal curvature, anterior chamber depth, lens thickness, and axial length.
Lab products found in correlation
21 protocols using lenstar
Visual Acuity and Ocular Biometrics
Visual acuity was measured with the participant's habitual correction. All participants had a best corrected visual acuity of 20/25 or better. Non-cycloplegic autorefraction was measured for both eyes (WAM-5000; Grand Seiko, Tokyo, Japan). Axial length and central corneal thickness were measured using a non-contact low-coherence optical biometer (LenStar; Haag-Streit, Köniz, Switzerland). Five measurements were collected and averaged for each eye. Exclusion criteria included any ocular pathology, use of prescription or over-the-counter medications known to affect sleep or circadian rhythms, use of sleep aids such as melatonin, and shift work or travel across more than two time zones during the month prior to the study visit. No participants had any systemic disease with ocular manifestations, such as diabetes or hypertension.
Comprehensive Ophthalmic Measurements Protocol
Pupil Dynamics Under Mydriasis
Refractive Outcomes of Combined Procedures
Preoperative data were used to establish a baseline, which typically occurred in the visit immediately before surgery. Postoperatively, data were collected from the following time points to compare with baseline data: 1 day, 1 week, 1 month, 3 months, and 6 months. At each time point, the data collected included IOP, number, and type of medications used, and manifest refraction was obtained at certain time points.
Comprehensive Examination Protocol for Diabetes
Cycloplegic Refraction Measurement Protocol
Ocular Biometry in Healthy Adults
Noncontact Ocular Biometry with Lenstar
Ocular Imaging and Pupillometry Protocol
Biometric Measurements for AOSLO Imaging
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