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Changes in anterior chamber characteristics measured with a dual Scheimpflug analyzer and an anterior segment optical coherence tomography after laser in situ keratomileusis for myopia

Does laser in situ keratomileusis (LASIK) surgery affect anterior chamber characteristics measured with a dual Scheimpflug analyzer and an anterior segment optical coherence tomography in myopic patients?

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612001200875
Enrollment
80
Registered
2012-11-14
Start date
2011-11-10
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Laser in situ keratomileusis (LASIK) has been proven to be safe and effective for correction of myopia and myopic astigmatism. However, postoperative complications such as iatrogenic corneal protrusion occasionally occurred. Given that the position of the lens is unchangeable after refractive surgery, the corneal protrusion should be associated with structural changes of the anterior segment such as deepening of the anterior chamber depth. Most of the previous studies mainly focused on the central or midperipheral anterior chamber structure, but ignored the changes of peripheral anterior chamber parameters post-LASIK. In the present study, we plan to investigate the anterior chamber characteristics changes after LASIK not only in terms of central anterior chamber structure, but also in terms of peripheral anterior chamber angles. The purpose is to evaluate the effects of LASIK surgery on anterior ocular structures.

Interventions

In this study, all participants undergo standard laser in situ keratomileusis (LASIK) surgery in both eyes only once. The LASIK procedures are performed in each eye by first creating a superiorly hinged corneal flap using the Hansatome microkeratome with a 160 micron m head and 8.5 mm ring. The laser ablation is performed using excimer Laser with a goal of emmetropia. The surgery procedures usually takes about 20 minutes for each patient. The central anterior chamber depth (ACD), anterior chambe

In this study, all participants undergo standard laser in situ keratomileusis (LASIK) surgery in both eyes only once. The LASIK procedures are performed in each eye by first creating a superiorly hinged corneal flap using the Hansatome microkeratome with a 160 micron m head and 8.5 mm ring. The laser ablation is performed using excimer Laser with a goal of emmetropia. The surgery procedures usually takes about 20 minutes for each patient. The central anterior chamber depth (ACD), anterior chamber volume (ACV), average radius of posterior axial curvature (ARPAC) are measured using the Galilei Scheimpflug analyser. Measurements with the dual Scheimpflug analyzer are performed according to the manufacturer’s guidelines. The device is brought into focus and the subject’s eye is aligned along the visual axis by a central fixation light. The subjects are asked to sit back after each measurement, and the device is realigned before each measurement.The superior, inferior, nasal, temporal anterior chamber angles (ACAs) are respectively measured using Visante anterior segment optical coherence tomography (AS-OCT). Scans of the ACAs of each eye are obtained at the 3 and 9 o’clock positions (horizontal), and at the 6 and 12 o’clock positions (vertical). Subjects are instructed to blink prior to all measurements and open their eyes wide during scan acquisition. As the eyelids may interfere with AS-OCT image acquisition of the ACA at 6 and 12 o’clock positions, the upper and lower lids are gently moved out of the way to image the superior and inferior angle- taking care to avoid inadvertent pressure on the globe. Measurements using the Galilei and Visante AS-OCT are taken before and 2 weeks and 2 months after LASIK. Each measurement needs about 5 minutes.

Sponsors

Zhong Xingwu
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Myopic patients with stable refraction for at least 2 years, no contact lens wear for 2 weeks prior to the baseline examination

Exclusion criteria

history of following diseases: keratoconus or keratoconus suspect, corneal dystrophy, ocular trauma, diabetes, retinal disease, glaucoma and severe dry eye disease

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026