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Observing the stability of Indian eye lens made from hydrophobic material

Toric Stability of a Hydrofobic Acrylate Co Polymer Toric Intra Ocular Lens - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/05/086860
Enrollment
50
Registered
2025-05-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: H259- Unspecified age-related cataract

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

Dr Yamini Bharti
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with age related cataract requiring surgical intervention Patients who have with the rule corneal astigmatism of more than 1 diopter Patients in whom Magnificent Toric IOL has been implanted Patient who are willing to comply with the follow up requirements Patients who are not the part of any other study Patients who are treatment naive Patients who have not undergone any kind of ocular surgery Age above 40 years onwards

Exclusion criteria

Exclusion criteria: Presence of irregular corneal astigmatism or astigmatism less than 1 diopter Co existing ocular diseases such as glaucoma, diabetic retinopathy, uveitis, corneal opacity Systemic conditions like wheel chair patients, parkinsonism Psychiatric conditions like dementia Patients with prior ocular trauma Patients with prior ocular surgery or any vitreoretinal surgery Age less than 40 years Poorly dilating pupils Patients who might be loss to follow up

Design outcomes

Primary

MeasureTime frame
To evaluate the rotational stability of the Magnificent Toric IOLTimepoint: At 1week, 1month, 3months postoperatively

Secondary

MeasureTime frame
To assess uncorrected and best corrected visual acuity outcomes To measure residual refractive astigmatism at each follow up visit To evaluate patient reported satisfaction and visual outcomes using a validated questionnaire To monitor for postoperative complications such as IOL decentrationTimepoint: At 1week, 1month, 3months postoperatively

Countries

India

Contacts

Public ContactMaj Gen Dr Sagarika Patyal

Centre For Sight Eye Institute, Dwarka

sagarikapatyal@gmail.com9643437024

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026