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Comparison of Visual Results and Lens Stability of Extended Depth of Focus Toric Intraocular Lenses with Two Different Sizes

Clinical Outcomes and Rotational Stability of EDOF Toric lens using two Different sized IOLs - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102183
Enrollment
160
Registered
2026-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: H258- Other age-related cataract

Interventions

Intervention1: To compare the postoperative rotational stability of toric EDOF intraocular lenses implanted in pseudophakic eyes using two different lens diameters selected according to the patient s

Sponsors

Nethradhama Super Speciality Eye Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 2. Patients undergoing cataract surgery for both eyes. 3. Eyes planned for pseudophakic implantation of a toric EDOF IOL. Preoperative corneal regular astigmatism less than 0.75 D and less than 3.50 D suitable for toric correction. WTW measurement taken from IOLMaster 700 optical biometer. Axial length between 22.0 mm and 26.0 mm. Clear cornea and normal anterior segment anatomy. Ability to attend follow-up visits for at least 3 months postoperatively.

Exclusion criteria

Exclusion criteria: 1. History of other ocular surgeries in the study eye. 2. Irregular corneal astigmatism or corneal pathology. 3. Glaucoma with uncontrolled intraocular pressure or optic nerve damage. 4. Retinal pathology affecting visual potential. 5. Anterior segment anomalies along with zonular instability, capsular bag abnormalities, or pseudoexfoliation that may interfere with IOL implantation or rotation assessment. 6. Pupillary abnormalities. 7. Intraoperative complications (e.g., posterior capsular rupture, vitreous loss). 8. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
To compare the postoperative rotational stability of toric EDOF intraocular lenses implanted in pseudophakic eyes using two different lens diameters selected according to the patient s IOL Diopteric power.Timepoint: 1 day, day 15, and 3 months

Secondary

MeasureTime frame
1. To assess the visual outcomes (uncorrected and corrected distance, intermediate, and near visual acuity) with the two different lens diameters. 2. To evaluate refractive predictability and residual astigmatism following implantation. 3. To determine patient satisfaction and visual quality, including the presence of photic phenomena (glare, halos, starbursts). 4. To analyze correlations between WTW measurements, axial length, and IOL Diopteric power. 5. To assess any IOL-related complications (decentration, tilt, or need for repositioning). Timepoint: 1 day, day 15, and 3 months

Countries

India

Contacts

Public ContactDrSuchetha

Nethradhama Super Speciality Eye Hospital

Suchithrasuzi007@gmail.com8129193309

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026