Skip to content

Rotational Stability of Different Intraocular Lenses in The Capsular Bag

Rotational Stability of Different Intraocular Lenses in The Capsular Bag

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03761745
Enrollment
40
Registered
2018-12-03
Start date
2018-12-29
Completion date
2024-10-30
Last updated
2025-03-28

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

Conditions

Intraocular Lens Complication, Phacoemulsification

Keywords

Rotation, Postoperative Care

Brief summary

To evaluate the rotational stability difference among different intraocular lens. The rotational stability is evaluated by measurement of rotation of the IOL after surgery.

Interventions

None listed

Sponsors

Wenzhou Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Patients who had received Femtosecond laser-assisted phacoemulsification surgery with IntelliAxis-L capsular mark. * The operation was smooth and there were no surgical complications.

Exclusion criteria

* Corneal and other ocular diseases (such as corneal opacity, keratitis, glaucoma, uveitis, lens dislocation or subluxation, lens capsule relaxation, retinopathy, etc.); * History of ocular trauma or surgery before this cataract surgery; * intraoperative and postoperative complications, such as posterior capsule rupture, corneal endothelium decompensation; * Patients with severe or unstable heart, liver, kidney, lung, endocrine (including thyroid dysfunction), blood, mental dysfunction and other diseases affect the results of this study;

Design outcomes

Primary

MeasureTime frameDescription
Alignment of intraocular lens1 day postoperativelyThe alignment of intraocular lens was evaluated by anterior segment photography

Secondary

MeasureTime frameDescription
Intraocular Pressure1 day, 1 week, 1 month, postoperativelyIntraocular Pressure measured by non-contact tonometers
Corrected Visual Acuity (UCVA) at Distance1 day, 1 week, 1 month, postoperativelyUCVA was determined by subjective refraction
Uncorrected Visual Acuity (UCVA) at Distance1 day, 1 week, 1 month, postoperatively

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026