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Evaluating the axial stability of Clareon IOL in short and long eyes

An evaluation of axial stability of Clareon IOL in short and long eyes: A single center, prospective, open-label study - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052810
Enrollment
60
Registered
2023-05-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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: Intraocular lens: Clareon Monofocal IOL implantation during Cataract surgery and patient is followed for 3 months Control Intervention1: Clareon Monofocal IOL: IOL - Clareon Autonome As

Sponsors

Alcon Laboratories Ind Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.All patients undergoing cataract surgery with Clareon IOL in the Axial length range less than 22.5mm Or Greater than 24.5mm 2.Preoperative or expected postoperative regular corneal astigmatism of 3.Age group 20 - 80 years

Exclusion criteria

Exclusion criteria: 1.Zonular weakness 2.Psuedoexfoliation 3.Post Refractive surgery 4.Cataract surgery combined with any other additional procedures 5.Intraoperative complications like Vitreous loss or Anterior capsular tear 6.Eye which had any other intraocular surgery prior to cataract surgery

Design outcomes

Primary

MeasureTime frame
Change in ACD last post-op visit(12 wk) â?? first post-op visit(1 wk)Timepoint: 1 year—

Secondary

MeasureTime frame
1.Monocular Uncorrected Visual acuity- Distance(6m), Intermediate (66cm) 2.Monocular Best corrected Distance Visual acuity 3.Residual refractive errorTimepoint: 1 year—

Countries

India

Contacts

Public ContactDr Rachapalle Reddi Sudhir

Ophthalmologist, Sankara Nethralaya

drrrs@snmail.org

Outcome results

None listed

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