Cataract Clinical Trial
Official title:
Retrospective Evaluation of the Accuracy and Safety of the LaserArcs Femtosecond Cataract Surgery Arcuate Incision Nomogram in Patients Undergoing Cataract Surgery and Astigmatism Reduction
NCT number | NCT05278442 |
Other study ID # | 2109 LaserArc |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | April 1, 2022 |
Est. completion date | August 8, 2022 |
Verified date | October 2022 |
Source | Research Insight LLC |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Evaluation of the Accuracy and Safety of the LaserArcs Femtosecond Cataract Surgery Arcuate Incision Nomogram in Patients Undergoing Cataract Surgery and Astigmatism Reduction
Status | Completed |
Enrollment | 50 |
Est. completion date | August 8, 2022 |
Est. primary completion date | August 7, 2022 |
Accepts healthy volunteers | |
Gender | All |
Age group | 22 Years and older |
Eligibility | Inclusion Criteria: - Patients with cataract and otherwise healthy eyes, not exhibiting any significant ocular morbidity that would be expected to influence outcome measures. - Patients who are 22 years of age or older - Patients whose preoperative astigmatism was greater than 0.5 D - Patients who were implanted with a non-toric IOL. - Patients whose laser astigmatic keratotomy was planned using the LASER arcs nomogram Exclusion Criteria: - Patients with visually significant co-morbidities (corneal, retina, optic nerve disease) that could affect their satisfaction with surgery - Patients with surgical complications either during or after surgery (capsule tears, iris trauma, decentered IOL, cystoid macular edema, etc.) that would, in the judgment of the investigator, influence the outcome measures of the study. - Patients with previous refractive surgery within the past 6 months prior to cataract surgery |
Country | Name | City | State |
---|---|---|---|
United States | Quantum Vision Centers | Belleville | Illinois |
Lead Sponsor | Collaborator |
---|---|
Research Insight LLC |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Exploratory Endpoint - Postoperative manifest refraction cylinder and axis is the measured magnitude of spherical and cylindrical refraction at the postoperative visit. | Postoperative manifest refraction for sphere, cylinder, and axis. | Up to 3 months | |
Primary | Primary Endpoint -Postoperative magnitude of manifest astigmatism (diopters) divided by preoperative magnitude of manifest astigmatism (diopters) | Percent change in absolute magnitude of astigmatism | Up to 3 months | |
Secondary | Mean Attempted vs Achieved Correction (see description) | Mean attempted vs achieved correction. Attempted correction=postop target astigmatism-pre-op corneal astigmatism), achieved correction=postop manifest cylinder-pre-op corneal astigmatism, attempted vs achieved=achieved correction-attempted correction mean attempted vs achieved=average of all individual calculated values for attempted vs achieved correction | Up to 3 months | |
Secondary | Secondary Endpoint - Standard deviation of attempted vs achieved correction = standard deviation of of all individual calculated values for attempted vs achieved correction | Standard deviation of attempted vs number of achieved correction of corneal astigmatism. | Up to 3 months |
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