Refractive Outcomes Utilizing Two SS-OCT Biometers for IOL Power Calculations

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The purpose of this study is to evaluate and compare the potential refractive outcomes using the Argos 1.5 biometer in the surgical planning for cataract extraction to that obtained from IOLMaster 700. Both devices are used as standard of care in surgical planning optimization for patients undergoing cataract surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Healthy Volunteers: f
View:

• 21 years or older (Adult age)

• Assessed to have Cataract Grade 1 and above per LOCS III or Wisconsin Grading scale in at least one eye.

• Able to comprehend and sign the informed consent form.

• Potential postoperative best corrected distance visual acuity (BCDVA) of 0.3 logMAR or better and targeted post-op refraction to be emmetropia, based on the investigator expert medical opinion.

Locations
United States
Utah
The Eye Institute of Utah
RECRUITING
Salt Lake City
Contact Information
Primary
Lexi L Guild
lguild@theeyeinstitute.com
8012635705
Backup
Allison Hales
ahales@theeyeinstitute.com
8012635735
Time Frame
Start Date: 2025-01-09
Estimated Completion Date: 2025-02-22
Participants
Target number of participants: 50
Treatments
Observational
No interventions will be administered.
Related Therapeutic Areas
Sponsors
Collaborators: Alcon Research
Leads: The Eye institute of Utah

This content was sourced from clinicaltrials.gov