Hybrid SA RGP Center/S-H Skirt Daily Wear 90 Day Multicenter Study

This study has been completed.
Sponsor:
Information provided by:
SynergEyes, Inc.
ClinicalTrials.gov Identifier:
NCT00804505
First received: December 8, 2008
Last updated: December 22, 2009
Last verified: December 2009

December 8, 2008
December 22, 2009
June 2008
November 2008   (final data collection date for primary outcome measure)
  • Comparison of objective findings (slit lamp, lens fitting, deposits, subjective symptoms, adverse events test vs control [ Time Frame: 3 months ] [ Designated as safety issue: Yes ]
  • Visual acuity comparison test/control. [ Time Frame: 3 mo. ] [ Designated as safety issue: No ]
Not Provided
Complete list of historical versions of study NCT00804505 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Hybrid SA RGP Center/S-H Skirt Daily Wear 90 Day Multicenter Study
A 90 Day Multi-Center, Randomized, Parallel Group Daily Wear Investigation of a New Hybrid Lens SynergEyes SA Manufactured With a Rigid Gas Permeable Center (Petrafocon A) and a Silicone Hydrogel Skirt (Larafilcon A) Compared to SynergEyes A (Paflufocon D Hem-iberfilcon A)

The purpose of the study is to demonstrate that the SynergEyes SA Hybrid Contact Lens clinical performance is substantially equivalent to that of the SynergEyes A Hybrid Lens when studied:

  • within the corresponding range of lens powers
  • in a population randomized within multiple investigational sites
  • with a study ration of 2/1 test vs control lenses
  • for a duration of 90 days.

The objective of the study is to compare the SynergEyes SA Hybrid Contact Lens (Test) to the SynergEyes A Hybrid Contact lens (Control) when used in a daily wear regimen on non-diseased eyes for the correction of myopia (-0.25 to -6.00Diopters) with up to -2.50 Diopters of astigmatism. The population will be randomized into a 2/1 ratio of the Test/Control for 90 days. The study objective is to complete at least 40 subjects in the Test material and 20 subjects in the Control material.

The purpose of the study is to demonstrate that the SynergEyes SA Hybrid Contact Lens clinical performance is substantially equivalent to that of the SynergEyes A Hybrid Lens when studied within the corresponding range of powers in a population randomized within investigational sites to produce a 2/1 ratio of Test vs. Control lenses.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Corneal Disease
  • Hypersensitivity
  • Device: SynergEyes Hybrid (petrafocon A hem-larafilcon A) Hybrid Contact Lens
    Comparison to control hybrid lens with similar 'dose'minimum 8 hours daily use for up to 90 days.
  • Device: SynergEyes Hybrid (paflufocon D hem-iberfilcon A) Contact Lens
    Comparison to test lens: Daily use for minimum 8 hours up to 90 days.
  • Experimental: 1
    Test arm daily wear hybrid contact lens.
    Intervention: Device: SynergEyes Hybrid (petrafocon A hem-larafilcon A) Hybrid Contact Lens
  • 2
    Control: SynergEyes Hybrid (paflufocon D hem-iberfilcon A) Hybrid Contact Lens
    Intervention: Device: SynergEyes Hybrid (paflufocon D hem-iberfilcon A) Contact Lens
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
98
December 2008
November 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

Prior to being considered eligible to participate in this study, each subject MUST:

  1. Be at least 18 years of age as of the date of evaluation.
  2. Have

    1. read the Informed Consent,
    2. been given an explanation of the Informed Consent,
    3. indicated an understanding of the Informed Consent and
    4. signed the Informed Consent Form.
  3. Be willing and able to adhere to the instructions set forth in this protocol and able to keep all specified appointments.
  4. Be a current contact lens wearer.
  5. Possess wearable and visually functional eyeglasses.
  6. Be in good general health, based on his/her knowledge.
  7. Require spectacle lens powers between plano and -6.00 diopters sphere with no more than -2.50 diopters of spectacle refractive astigmatism and be willing to wear lenses in both eyes.
  8. Have manifest refraction visual acuity equal to or better than 20/25 in each eye.

Exclusion Criteria:

  • Subjects may not be enrolled into the study if ANY of the following apply:

    1. Subject is wearing lenses in a monovision modality and is unwilling to be fit with distance lenses in both eyes. NOTE: Subjects may NOT wear monovision lenses at any time during the study as it will interfere with the distance visual acuity measurement.
    2. Subject exhibits poor personal hygiene.
    3. Subject is currently or within 30 days prior to this study has been an active participant in another clinical study.
    4. Subject is currently pregnant (to the best of the subject's knowledge), is planning a pregnancy within the next 3 months or is lactating.
    5. Subject is a member, relative or household member of the office staff, including the investigator(s).
    6. Subject has a known sensitivity to ingredients used in contact lens care products or over-the-counter lubricants and artificial tears.
    7. Subject has undergone refractive surgery or is currently receiving or has previously received orthokeratology treatment.
    8. Subject is aphakic or pseudophakic.
    9. Subject has ocular or systemic disease such as, but not limited to: anterior uveitis or iritis (past or present), glaucoma, Sjögren's syndrome lupus erythematosus, scleroderma, keratoconus or type II diabetes.
    10. Use of ocular medications for any reason or systemic medications which might interfere with contact lens wear.
    11. A known history of corneal hypoesthesia (reduced corneal sensitivity).
    12. Slit lamp findings that would contraindicate contact lens wear, including but not limited to:

      • History of corneal ulcer, corneal infiltrates or fungal infections
      • Corneal scars within the visual axis
      • Pterygium
      • Dry eye symptoms with decrease tear levels and punctate staining ≥ Grade 2
      • Neovascularization or ghost vessels > 1.5 mm in from the limbus
      • Seborrhoeic eczema, seborrhoeic conjunctivitis
      • History of papillary conjunctivitis that has interfered with lens wear or a current condition of Grade 2 (Mild) or greater
    13. Clinically significant (Grade 3 or 4) anterior segment abnormalities or any infection of the eye, lids, or associated structures.

TO BE ELIGIBLE TO BE RANDOMIZED FOR STUDY PRODUCT TRIAL A SUBJECT MUST HAVE ALL OF THE INCLUSION CRITERIA AND NONE OF THE EXCLUSION CRITERIA PRESENT.

TO BE ELIGIBLE FOR LENS DISPENSING, THE SUBJECT'S STUDY DEVICE CONTACT LENS VISUAL ACUITY MUST BE EQUAL TO OR BETTER THAN 20/30 IN EACH EYE

Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00804505
SI-0804 V1.0
No
SynergEyes, Inc., Joe Collins
SynergEyes, Inc.
Not Provided
Study Director: William Gleason, OD Foresight Regulatory Strategies, Inc.
SynergEyes, Inc.
December 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP