Ten-year Follow-up of Laser in Situ Keratomileusis in Patients 8 to 15 Years Old

I

Instituto de Olhos de Goiania

Status and phase

Completed
Phase 4

Conditions

Anisometropia

Treatments

Procedure: LASIK

Study type

Interventional

Funder types

Other

Identifiers

NCT00800774
ARVO - BN - 2009

Details and patient eligibility

About

The purpose of this study is to determine the safety, efficacy, predictability, and stability of laser in situ keratomileusis (LASIK) to correct high anisometropia in patients 8 to 15 years old in whom conventional treatments have failed.

Full description

Nine eyes of nine patients (3 male and 6 female) with high anisometropia (>3.50 D), were included in this study. Minimum follow-up was 10 years. All patients were treated with the Chiron Technolas 217 excimer laser.

Enrollment

9 patients

Sex

All

Ages

8 to 15 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • High anisometropia (>3.50 D)
  • Patients 8 to 15 years old
  • Conventional treatments have failed

Exclusion criteria

  • Diabetes
  • Autoimmune diseases
  • Topographic abnormalities

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

9 participants in 1 patient group

1
Experimental group
Description:
Nine eyes of nine patients (3 male and 6 female) with high anisometropia (>3.50 D), were included in this study. Minimum follow-up was 10 years. All patients were treated with the Chiron Technolas 217 excimer laser.
Treatment:
Procedure: LASIK

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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