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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05461586
Other study ID # MDEV104MREE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 14, 2022
Est. completion date August 9, 2022

Study information

Verified date January 2023
Source Johnson & Johnson Surgical Vision, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Prospective, multi-center, non-interventional, randomized, comparative clinical study to identify an optimal refractive technique that provides maximum plus refractive endpoint for best corrected distance visual acuity (BCDVA).


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date August 9, 2022
Est. primary completion date August 9, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Participant in PCOL-102-AHSF who were bilaterally implanted with TECNIS IOL, Models C1V000, C2V000 or ICB00 and have completed and are at least 30 days postoperative from their second eye surgery; 2. At least one implanted eye with clear ocular media; 3. Signed informed consent and HIPAA authorization or equivalent documentation necessary to comply with applicable privacy laws pertaining to medical treatment in Australia and New Zealand; 4. Availability, willingness and sufficient cognitive awareness to comply with examination procedures. Exclusion Criteria: 1. Best-corrected distance visual acuity (BCDVA) worse than 0.66 decimal (6/9 or 20/30 Snellen); 2. Subjects with ongoing adverse events that might impact outcomes during the study visit as determined by the investigator.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Refractive Technique (MR #1)
Fogging method that employs fogging lens to ensure there is sufficient visual defocus to induce blur.
Refractive Technique (MR #2)
Duochrome method that employs the chromatic aberration of the eye, with the shorter wavelengths (green) focused in front of the longer (red) wavelengths

Locations

Country Name City State
Australia Sunshine Eye Clinic Birtinya Queensland

Sponsors (1)

Lead Sponsor Collaborator
Johnson & Johnson Surgical Vision, Inc.

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference between two manifest refractive techniques on outcome variable MRSE Refractive technique 1 will use a plus lens fogging technique and refractive technique 2 will use the Duochrome technique to achieve maximum plus refraction for best-corrected visual acuity (BCDVA). Day 0
Primary Difference between two manifest refractive techniques on visual acuity Refractive technique 1 will use a plus lens fogging technique and refractive technique 2 will use the Duochrome technique to achieve maximum plus refraction for best-corrected visual acuity (BCDVA). Day 0
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