search
Back to results

Comparison of Clinical Outcomes of Small-incision Lenticule Extraction (SMILE) Between Different Cap Thickness.

Primary Purpose

Myopia

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
SMILE using 120μm cap thickness
SMILE using 140μm cap thickness
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myopia focused on measuring Small incision lenticule extraction, Cap thickness

Eligibility Criteria

20 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. age of 20 years or older.
  2. Myopia
  3. Who is willing to get SMILE surgery

Exclusion Criteria:

  1. severe ocular surface disease
  2. any corneal disease, cataract, glaucoma, macular disease, or previous history of intraocular or corneal surgery
  3. Patients with suspicion of keratoconus on corneal topography

Sites / Locations

  • Department of Ophthalmology, Yonsei Univeristy College of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

120 μm group

140 μm group

Arm Description

The subjects underwent SMILE using 120 μm cap.

The subjects underwent SMILE using 140 μm cap.

Outcomes

Primary Outcome Measures

Uncorrected Distance Vision Acuity
Uncorrected Distance Vision Acuity in logMAR scale will be compared between the two groups at each time point.
Corrected Distance vision Acuity
Corrected Distance Vision Acuity in logMAR scale will be compared between the two groups at each time point.

Secondary Outcome Measures

1.Total higher order aberration at each time point between the two groups.
Total higher order aberrations, spherical aberrations, and coma aberrations are examined using Keratron Scout (Optikon 2000, Rome, Italy). The unit of those is "μm". 1,2. Total higher order aberrations at each time point and change from baseline at each time point will be compared between the two groups.
2.Total higher order aberration changes from baseline at each postoperative time point between the two groups.
Total higher order aberrations, spherical aberrations, and coma aberrations are examined using Keratron Scout (Optikon 2000, Rome, Italy). The unit of those is "μm". 1,2. Total higher order aberrations at each time point and change from baseline at each time point will be compared between the two groups.
3.Spherical aberration at each time point between the two groups.
3,4. Spherical aberrations at each time point and change from baseline at each time point will be compared between the two groups.
4.Spherical aberration changes from baseline at each postoperative time point between the two groups.
3,4. Spherical aberrations at each time point and change from baseline at each time point will be compared between the two groups.
5.Coma aberration at each time point between the two groups.
5,6. Coma aberrations at each time point and change from baseline at each time point will be compared between the two groups. Corneal biomechanics including deformation amplitude ratio (DA ratio), and stiffness parameter at first applanation (SP-A1) is examined using Corvis ST (Oculus, Wetzlar, Germany). The unit of SP-A1 is "mm Hg/mm", and DA ratio is unitless.
6.Coma aberration changes from baseline at each postoperative time point between the two groups.
5,6. Coma aberrations at each time point and change from baseline at each time point will be compared between the two groups. Corneal biomechanics including deformation amplitude ratio (DA ratio), and stiffness parameter at first applanation (SP-A1) is examined using Corvis ST (Oculus, Wetzlar, Germany). The unit of SP-A1 is "mm Hg/mm", and DA ratio is unitless.
7.Deformation amplitude ratio (DA ratio) at each time point between the two groups.
7,8 DA ratio at each time point and change from baseline at each time point will be compared between the two groups.
8.DA ratio changes from baseline at each postoperative time point between the two groups.
7,8 DA ratio at each time point and change from baseline at each time point will be compared between the two groups.
9.Stiffness parameter at first applanation (SP-A1) at each time point between the two groups.
9,10 SP-A1 at each time point and change from baseline at each time point will be compared between the two groups.
10.SP-A1 changes from baseline at each postoperative time point between the two groups.
9,10 SP-A1 at each time point and change from baseline at each time point will be compared between the two groups.

Full Information

First Posted
June 19, 2018
Last Updated
October 15, 2020
Sponsor
Yonsei University
search

1. Study Identification

Unique Protocol Identification Number
NCT03584555
Brief Title
Comparison of Clinical Outcomes of Small-incision Lenticule Extraction (SMILE) Between Different Cap Thickness.
Official Title
Comparison of Clinical Outcomes of Small-incision Lenticule Extraction (SMILE) Between Different Cap Thickness.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
March 18, 2017 (Actual)
Primary Completion Date
August 26, 2019 (Actual)
Study Completion Date
August 26, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In the past two decades, the femtosecond laser (FSL) technology has been introduced in the corneal refractive surgery filed, and brought a remarkable innovation. It can make tissue dissection through photodisruption and plasma cavitation. Initially, the FSL was used predominantly to make a corneal flap when performing laser in situ keratomileusis (LASIK), which is followed by stromal ablation using excimer laser. A new surgical technique called femtosecond lenticule extraction (FLEx) has been developed that uses only FSL to dissect two interfaces to create refractive lenticule and then remove it, which is very similar with LASIK. Small incision lenticule extraction (SMILE) which is the advanced form of all-in-one FSL refractive technique does not make a corneal flap rather make small incision where the separated refractive lenticule is removed through, and the upper part of the corneal tissue is called cap. Since the clinical outcomes of SMILE were firstly published in 2011, SMILE has been widely used for correction of myopia or myopic astigmatism worldwide. SMILE provides excellent visual outcomes and has advantages including a lesser decrease in corneal sensitivity and absence of flap related complications compared to LASIK. Because corneal ectasia after refractive surgery is the one of most terrifying complication, corneal biomechanics has been drawn interests to many researchers and clinicians. Theoretically, SMILE may preserve corneal biomechanics better than LASIK, because the anterior stroma which is stiffer than the posterior stroma remains intact in SMILE. However, there are some controversies, because previous studies investigating corneal biomechanics have been reported inconsistent outcomes, although SMILE has been reported equal to or better than LASIK. Weakening of corneal biomechanics and iatrogenic corneal ectasia have also been reported after SMILE. In addition, because the tensile strength of cornea gradually decreases as it goes backwards, creating deeper refractive lenticule may result in stronger cornea by preserving more of anterior lamellae of the cornea. But on the contrary, leaving sufficient residual stromal bed has been known to be important in preventing iatrogenic corneal ectasia, hence creating thin cap may be effective and desirable. Although many researches have been investigated the difference in biomechanical response between SMILE and LASIK, there are few studies evaluating the dependence of cap thickness on postoperative biomechanical strength after SMILE. El-Massry et al. reported that the thicker cap thickness showed higher postoperative corneal hysteresis (CH) and corneal resistance factor (CRF) with Ocular Response Analyzer (ORA; Reichert Ophthalmic Instruments, Depew, NY) which may not be optimal for a clear description of the viscosity and elasticity of the cornea,3 ; however, other studies have been presented that there is no significant difference of corneal biomechanics with cap thickness. There is no comparative human study using Corvis ST (Oculus, Wetzlar, Germany) despite presence of the study using Corvis ST in rabbit eyes. Furthermore, no prospective study with large number of subjects has been performed to date.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
Small incision lenticule extraction, Cap thickness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Enrollment period : 24 months after IRB approval Methods: The subjects are randomly divided into two groups. One group underwent SMILE surgery using 120 μm cap thickness, and the other group underwent SMILE surgery using 140 μm cap thickness. Before surgery, all patients underwent a detailed ophthalmological examination that included evaluation of logarithm of the minimum angle of resolution (logMAR) uncorrected-distance visual acuity (UDVA) and CDVA, manifest refraction, slit-lamp examination (Haag-Streit, Köniz, Switzerland), keratometry, and Scheimpflug-based corneal topography (Pentacam HR, Oculus). Dynamic corneal response (DCR) parameters were examined using Corvis ST. Corneal wavefront aberrations were measured using Keratron Scout (Optikon 2000, Rome, Italy). All examinations were repeated at 1, 3, and 6 months after surgery.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
120 μm group
Arm Type
Active Comparator
Arm Description
The subjects underwent SMILE using 120 μm cap.
Arm Title
140 μm group
Arm Type
Active Comparator
Arm Description
The subjects underwent SMILE using 140 μm cap.
Intervention Type
Procedure
Intervention Name(s)
SMILE using 120μm cap thickness
Intervention Description
The surgery was performed with standardized techniques with triple centration technique using the 500-KHz VisuMax system (Carl Zeiss Meditec AG, Jena, Germany). The superior cap depth was set as 120 or 140 µm, and the length of the side cut was set to 2 mm. Once the anterior (upper) and posterior (lower) planes of the lenticule were defined, the anterior and posterior interfaces were dissected using a micropetala with a blunt circular tip and extracted with midforceps. The integrity of the lenticule was assessed subsequently.
Intervention Type
Procedure
Intervention Name(s)
SMILE using 140μm cap thickness
Intervention Description
The surgery was performed with standardized techniques with triple centration technique using the 500-KHz VisuMax system (Carl Zeiss Meditec AG, Jena, Germany). The superior cap depth was set as 120 or 140 µm, and the length of the side cut was set to 2 mm. Once the anterior (upper) and posterior (lower) planes of the lenticule were defined, the anterior and posterior interfaces were dissected using a micropetala with a blunt circular tip and extracted with midforceps. The integrity of the lenticule was assessed subsequently.
Primary Outcome Measure Information:
Title
Uncorrected Distance Vision Acuity
Description
Uncorrected Distance Vision Acuity in logMAR scale will be compared between the two groups at each time point.
Time Frame
from preoperative to postoperative 6 months
Title
Corrected Distance vision Acuity
Description
Corrected Distance Vision Acuity in logMAR scale will be compared between the two groups at each time point.
Time Frame
from preoperative to postoperative 6 months
Secondary Outcome Measure Information:
Title
1.Total higher order aberration at each time point between the two groups.
Description
Total higher order aberrations, spherical aberrations, and coma aberrations are examined using Keratron Scout (Optikon 2000, Rome, Italy). The unit of those is "μm". 1,2. Total higher order aberrations at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months
Title
2.Total higher order aberration changes from baseline at each postoperative time point between the two groups.
Description
Total higher order aberrations, spherical aberrations, and coma aberrations are examined using Keratron Scout (Optikon 2000, Rome, Italy). The unit of those is "μm". 1,2. Total higher order aberrations at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months
Title
3.Spherical aberration at each time point between the two groups.
Description
3,4. Spherical aberrations at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months
Title
4.Spherical aberration changes from baseline at each postoperative time point between the two groups.
Description
3,4. Spherical aberrations at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months
Title
5.Coma aberration at each time point between the two groups.
Description
5,6. Coma aberrations at each time point and change from baseline at each time point will be compared between the two groups. Corneal biomechanics including deformation amplitude ratio (DA ratio), and stiffness parameter at first applanation (SP-A1) is examined using Corvis ST (Oculus, Wetzlar, Germany). The unit of SP-A1 is "mm Hg/mm", and DA ratio is unitless.
Time Frame
from preoperative to postoperative 6 months
Title
6.Coma aberration changes from baseline at each postoperative time point between the two groups.
Description
5,6. Coma aberrations at each time point and change from baseline at each time point will be compared between the two groups. Corneal biomechanics including deformation amplitude ratio (DA ratio), and stiffness parameter at first applanation (SP-A1) is examined using Corvis ST (Oculus, Wetzlar, Germany). The unit of SP-A1 is "mm Hg/mm", and DA ratio is unitless.
Time Frame
from preoperative to postoperative 6 months
Title
7.Deformation amplitude ratio (DA ratio) at each time point between the two groups.
Description
7,8 DA ratio at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months
Title
8.DA ratio changes from baseline at each postoperative time point between the two groups.
Description
7,8 DA ratio at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months
Title
9.Stiffness parameter at first applanation (SP-A1) at each time point between the two groups.
Description
9,10 SP-A1 at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months
Title
10.SP-A1 changes from baseline at each postoperative time point between the two groups.
Description
9,10 SP-A1 at each time point and change from baseline at each time point will be compared between the two groups.
Time Frame
from preoperative to postoperative 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age of 20 years or older. Myopia Who is willing to get SMILE surgery Exclusion Criteria: severe ocular surface disease any corneal disease, cataract, glaucoma, macular disease, or previous history of intraocular or corneal surgery Patients with suspicion of keratoconus on corneal topography
Facility Information:
Facility Name
Department of Ophthalmology, Yonsei Univeristy College of Medicine
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29610851
Citation
Damgaard IB, Ivarsen A, Hjortdal J. Refractive Correction and Biomechanical Strength Following SMILE With a 110- or 160-mum Cap Thickness, Evaluated Ex Vivo by Inflation Test. Invest Ophthalmol Vis Sci. 2018 Apr 1;59(5):1836-1843. doi: 10.1167/iovs.17-23675.
Results Reference
background
PubMed Identifier
29615281
Citation
Fernandez J, Rodriguez-Vallejo M, Martinez J, Tauste A, Pinero DP. Corneal biomechanics after laser refractive surgery: Unmasking differences between techniques. J Cataract Refract Surg. 2018 Mar;44(3):390-398. doi: 10.1016/j.jcrs.2017.10.054. Epub 2018 Mar 31.
Results Reference
background
PubMed Identifier
29053560
Citation
Weng S, Liu M, Yang X, Liu F, Zhou Y, Lin H, Liu Q. Evaluation of Human Corneal Lenticule Quality After SMILE With Different Cap Thicknesses Using Scanning Electron Microscopy. Cornea. 2018 Jan;37(1):59-65. doi: 10.1097/ICO.0000000000001404.
Results Reference
background
PubMed Identifier
27655417
Citation
He M, Wang W, Ding H, Zhong X. Comparison of Two Cap Thickness in Small Incision Lenticule Extraction: 100mum versus 160mum. PLoS One. 2016 Sep 21;11(9):e0163259. doi: 10.1371/journal.pone.0163259. eCollection 2016.
Results Reference
background
PubMed Identifier
27467038
Citation
Liu M, Zhou Y, Wu X, Ye T, Liu Q. Comparison of 120- and 140-mum SMILE Cap Thickness Results in Eyes With Thick Corneas. Cornea. 2016 Oct;35(10):1308-14. doi: 10.1097/ICO.0000000000000924.
Results Reference
background
PubMed Identifier
26266430
Citation
El-Massry AA, Goweida MB, Shama Ael-S, Elkhawaga MH, Abdalla MF. Contralateral Eye Comparison Between Femtosecond Small Incision Intrastromal Lenticule Extraction at Depths of 100 and 160 mum. Cornea. 2015 Oct;34(10):1272-5. doi: 10.1097/ICO.0000000000000571.
Results Reference
background

Learn more about this trial

Comparison of Clinical Outcomes of Small-incision Lenticule Extraction (SMILE) Between Different Cap Thickness.

We'll reach out to this number within 24 hrs