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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03202485
Other study ID # TICL compare with ICL+AK
Secondary ID
Status Completed
Phase N/A
First received June 22, 2017
Last updated June 27, 2017
Start date March 3, 2014
Est. completion date January 1, 2017

Study information

Verified date June 2017
Source Wenzhou Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the outcomes of a toric Implantable Collamer Lens (ICL) and a spherical Implantable Collamer Lens combined with astigmatic keratotomy (AK) in the correction of high myopic astigmatism.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date January 1, 2017
Est. primary completion date March 2, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- age ranged from 18 to 40 years,

- myopia greater than -8.00 diopters (D), and refractive cylinder in the range of 1.50D to 5.50D,

- for the patients who were planned to undergo AK+ICL implantation, the axial difference between the corneal astigmatism and the manifest refractive astigmatism was less than 10 degree,

- a stable refractive error during the previous 2 years,

- anterior chamber depth more than 2.8 mm,

- endothelial cell density (ECD) more than 2500 cells/mm2, and

- scotopic pupillary diameter less than 7 mm.

Exclusion Criteria:

- subjects had significant irregular astigmatism, corneal pathological changes, glaucoma, ocular inflammation, or previous ocular trauma or surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Toric Implantable Collamer Lens
uses Toric Implantable Collamer Lens implantation to correct the high myopic astigmatism.
ICL + Astigmatic keratotomy
uses Implantable Collamer Lens implantation combined with Astigmatic keratotomy to correct the high myopic astigmatism

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wenzhou Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary Uncorrected Visual Acuity (UCVA) at distance measured at 5 meter 2 years after surgery
Primary astigmatism astigmatism getting from subjective refraction 2 years after surgery
Secondary Best Corrected Visual Acuity (BCVA) at distance subjective refraction 2 years after surgery
Secondary Spherical Equivalent (SE) subjective refraction 2 years after surgery
Secondary mean postoperative BCVA/mean preoperative BCVA safety index 2 years after surgery
Secondary mean postoperative UCVA/mean preoperative BCVA efficacy index 2 years after surgery
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