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Trials / Recruiting

RecruitingNCT07453992

Postoperative Rotational Dynamics of Three Toric Intraocular Lens Designs

Postoperative Rotational Dynamics of Different Toric Intraocular Lens Designs

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
Jin Yang · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This prospective comparative cohort study evaluates and compares postoperative rotational stability and time-course dynamics of three commercially available toric intraocular lenses (TECNIS Toric II \[ZCU\], AcrySof IQ Toric, and AT TORBI 709M) after phacoemulsification cataract surgery. Rotation is quantified by registering postoperative retroillumination photographs to the end-of-surgery baseline using iris/scleral landmarks, with follow-up at postoperative day 1, day 3, week 1, week 2, month 1, and month 3. Associations between rotational outcomes and ocular biometric parameters are analyzed using linear mixed-effects models to inform individualized IOL selection and perioperative management.

Conditions

Interventions

TypeNameDescription
DEVICETECNIS Toric II (ZCU)Using TECNIS Toric II (ZCU) intraocular lens during standard phacoemulsification cataract surgery.
DEVICEAcrySof IQ ToricUsing AcrySof IQ Toric intraocular lens during standard phacoemulsification cataract surgery.
DEVICEAT TORBI 709MUsing the AT TORBI 709M intraocular lens during standard phacoemulsification cataract surgery.

Timeline

Start date
2025-01-01
Primary completion
2026-10-31
Completion
2030-12-31
First posted
2026-03-06
Last updated
2026-03-06

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07453992. Inclusion in this directory is not an endorsement.