Patient Preference and Visual Quality With Contralateral Synergy Versus Panoptix

Cataract Clinical Trial

Official title:

Patient Preference and Visual Quality With Contralateral Synergy Versus Panoptix

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05610540
• Other study ID #: FAB-1274
• Status: Completed
• Start date: April 12, 2022
• Est. completion date: May 31, 2023

Study information

• Verified date: July 2023
• Source: Bucci Laser Vision Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The goal of this study is to compare the visual quality and patient preference of the Synergy IOL versus the PanOptix IOL when one of each lens is placed in the same patient.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: May 31, 2023
• Est. primary completion date: February 21, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years and older

Eligibility

Inclusion Criteria:

• Bilateral cataracts for which phacoemulsification extraction and posterior IOL implantation have been planned for both eyes

• Desire to mitigate postoperative presbyopia with implantation of Synergy IOL in one eye and PanOptix Trifocal IOL in the opposite eye

Exclusion Criteria:

• Any vision-limiting problems (e.g., corneal, retinal, infection) which can potentially limit post-operative visual performance

• Any ocular condition or trauma that is not resolved, stable, or would compromise the well-being of the subject

Related Conditions & MeSH terms

• Cataract
• IOL
• Patient Satisfaction

Intervention

Device:
• TECNIS Synergy IOL
Implanted in one eye
• AcrySof PanOptix Trifocal IOL
Implanted in one eye

Locations

Country	Name	City	State
United States	Bucci Laser Vision Institute	Wilkes-Barre	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Bucci Laser Vision Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient Satisfaction - subjective questionnaire	Subjective questionnaire explores the frequency and need for glasses for various visual functions at distance, intermediate, and near and overall satisfaction of visual function without glasses	3 months to 18 months after cataract surgery
Primary	Visual Acuity at Distance	Uncorrected and best corrected visual acuities measured at distance	3 months to 18 months after cataract surgery
Primary	Visual Acuity at Intermediate	Uncorrected and best corrected visual acuities measured at intermediate	3 months to 18 months after cataract surgery
Primary	Visual Acuity at Near	Uncorrected and best corrected visual acuities measured at near	3 months to 18 months after cataract surgery