Skip to content

Comparison of visual outcomes ,patient satisfaction following bilateral insertion of Tecnis Synergy versus PanOptix trifocal intraocular lenses

Comparison of clinical results , functional outcomes and patient satisfaction following bilateral implantation of Tecnis Synergy versus PanOptix trifocal intraocular lenses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/038106
Enrollment
60
Registered
2021-11-17
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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: TECNIS SYNERGY IOL: IT IS AN INTRAOCULAR LENS INSERTED IN THE EYE AT THE TIME OF CATARACT SURGERY , THROUGH THE CLEAR CORNEA INCISION Control Intervention1: PANOPTIX IOL: IT IS AN IN

Sponsors

johnson and johnson
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)bilateral implantation 2)cataractous eyes with no comorbities 3)regular corneal topography and corneal astigmatism 4)preoperative corneal astigmatism of 5)patient desiring spectacle independence and having realistic expectation 6)availability ,willingness and sufficient cognitive awareness to comply with examination procedures 7)signed informed consent

Exclusion criteria

Exclusion criteria: 1)active ocular disease in operative eye for example chronic uveitis ,proliferative diabetic retinopathy ,chronic glaucoma unresponsive to medication , corneal endothelial cell insufficiency 2)subjects with any systemic disease that could increase operative risk or confound the outcome 3)pregnant or lactating or pregnancy at the time of enrollment 4)any patient who is taking part in another study involving ocular surgery 5)significant irregular corneal astigmatism 6)pupil abnormalities

Design outcomes

Primary

MeasureTime frame
1)manifest refraction 2)UDVA 3)CDVA 4)DCIVA 5)UIVA 6)DCNVA 7)UNVATimepoint: POST OP 1 WEEK , 1,3,6,12 MONTHS

Secondary

MeasureTime frame
1)BINOCULAR CORRECTED DEFOCUS CURVE 2)PCO RATE 3)CONTRAST SENSITIVITY 4)READING SPEEDS 5)PHOTIC PHENOMENA 7)PATIENT SATISFACTIONTimepoint: POST OP 1 WEEK , 1,3 ,6 12 MONTHS

Countries

India

Contacts

Public ContactDr Shadwala Bharti

Nethradhama superspeciality eye hospital

salgutisahiti@gmail.com91-9502381471

Outcome results

None listed

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