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Clinical Trials/ACTRN12611001141932
ACTRN12611001141932
Completed
未知

Assessment of effect of multifocal contact lenses on myopia progression rates in children and adolescents

Brien Holden Vision Institute0 sites20 target enrollmentNovember 1, 2011

Overview

Phase
未知
Intervention
Not specified
Conditions
Myopia
Sponsor
Brien Holden Vision Institute
Enrollment
20
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 1, 2011
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Brien Holden Vision Institute

Eligibility Criteria

Inclusion Criteria

  • have successfully participated in study IERP2007\-009
  • \-be able to read and comprehend English and give informed consent as demonstrated by signing a record of informed consent (or their parent(s)/legal guardian);
  • \-if under 18 years of age, be accompanied by their parent(s)/legal guardian when signing the informed consent form;
  • \-be willing to comply with the wearing and clinical trial visit schedule as directed by the investigator;
  • \-have ocular health findings considered to be normal” and which would not prevent the participant from safely wearing contact lenses;
  • \-have vision correctable to at least 6/9 (20/30\) or better in each eye with contact lenses;

Exclusion Criteria

  • \-pre\-existing ocular irritation that would preclude contact lens fitting;
  • \-an ocular condition that may preclude safe wearing of contact lenses;
  • \-an active corneal infection or any active ocular disease that would affect wearing of contact lenses;
  • \-a need for concurrent category S3 and above ocular medication up to 12 weeks prior to and during the trial;
  • \-any systemic disease that may affect ocular health. Conditions such as systemic hypertension do not automatically exclude prospective participants;
  • \-any systemic or topical medications up to 12 weeks prior to and during the trial that will affect ocular physiology or the performance of the lenses;
  • \-had eye surgery within 12 weeks immediately prior to enrolment for this trial;
  • \-undergone corneal refractive surgery;
  • \-any ocular injury or condition (including keratoconus and herpes keratitis) of the cornea, conjunctiva or eyelids that would affect the wearing of contact lenses;
  • \-contraindications to contact lens wear;

Outcomes

Primary Outcomes

Not specified

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