CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 115 enrolled
Drug / intervention
FS-LASIK 70 degree side-cut angle +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03122535
NCT03122535N/ACompleted
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70 Versus 110 Degrees Side-cut Angles in Femtosecond Laser-assisted in Situ Keratomileusis

University of Utah·interventional·Posted Apr 20, 2017·Updated May 28, 2021

In Brief

A clinical study evaluating FS-LASIK 70 degree side-cut angle and FS-LASIK 110 degree side-cut angle for Operative Incision. Completed, enrolled 115 participants across 1 site.

Detailed Summary

The purpose of this study is to compare 70 and 110 degree side-cut angles on the same patient undergoing Femtosecond Laser-assisted in Situ Keratomileusis (FS-LASIK).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOperative Incision
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedApr 20, 2017
Enrollment StartOct 7, 2014
Primary CompletionMar 21, 2019
TodayJul 2, 2026
Enrollment to primary: 4.5 yearsPosted 9.2 years ago

Interventions

FS-LASIK 70 degree side-cut angledevice

FS-LASIK surgical procedures will be performed according to the surgeons' standard practices. Patient will be masked as to the treatment they receive in either eye so as not to influence their subjective responses and visual measurements. Patients will be discontinued from the study if, on the day of surgery, both eyes cannot be randomized and operated as per protocol.

FS-LASIK 110 degree side-cut angledevice

FS-LASIK surgical procedures will be performed according to the surgeons' standard practices. Patient will be masked as to the treatment they receive in either eye so as not to influence their subjective responses and visual measurements. Patients will be discontinued from the study if, on the day of surgery, both eyes cannot be randomized and operated as per protocol.