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To evaluate the visual outcome of a new multifocal intraocular lens.

Assessment of visual performance of a new panfocal intraocular lens for visual quality and safety (Naturo, Caregroup, SS Pvt. Ltd.) - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/068178
Enrollment
50
Registered
2024-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: H251- Age-related nuclear cataract

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Caregroup, SS Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient with bilateral age related senile cataract 2. grade of cataract permitting optical biometry 3. no ocular/systemic contraindication for surgery 4. a patient with preoperative corneal astigmatism less than 1D in each eye 5. normal macular functions with normal anantomy of macula as seen on optical coherence tomography 6. no history or evidence of ocular anatomical or functional disorders other than cataract including strabismus neuro-ophthalmological disorders of optic nerve or high visual functions corneal pathologies disorders of uvea vitreous pathologies retinal disorders 7. no systemic contraindications to surgery under local anaesthesia 8. patient willing to undergo the investigations and comply with the follow-up schedule

Exclusion criteria

Exclusion criteria: 1. cataract precluding optical biometry 2. posterier-segment pathology 3. media opacity other than cataract 4. corneal higher order aberrations more than 0.3 micron as measured on ray-tracing wavefront aberrometer 5. patients with potential for intraoperative complications such as floppy iris syndrome and pseudo-exfoliation syndrome 6. cases where intra-operative complications compromise IOL placement with proper centration in the capsule bag 7. patient unwilling to undergo the required investigations or follow-up

Design outcomes

Primary

MeasureTime frame
1. visual acuity uncorrected & best corrected distance intermediate & near visual acuity 2. quality of visionTimepoint: 1. Pre-operative visit 2. Operative visit 3. Post-operative visit 1 - Day 1 4. Post-operative visit 2 - 1 month 3. Post-operative visit 3 - 3 months 3. Post-operative visit 4 - 6 months

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Namrata Sharma

Dr R P Centre for Ophthalmic Sciences

Namrata.sharma@gmail.com9810856988

Outcome results

None listed

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