Antibiotic drop instillation during continuous contact lens wear.

Phase 2

Completed

• Conditions: Contact lens wear; Eye - Normal eye development and function

• Registration Number: ACTRN12608000626369
• Lead Sponsor: CIBA VISION Corporation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2008-12-12
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Male
• Target Recruitment: 40

Inclusion Criteria

Be able to read and comprehend English and give informed consent as demonstrated by signing a record of informed consent;
Be at least 18 years old;
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 Snellen Visual Acuity of 6/12 (metres) or better in each eye with contact lenses, which means the participant can read within 3 lines of the nominal performance for human distance visiion (i.e. 6/6).
Be experienced at wearing contact lenses

Exclusion Criteria

Pre-existing ocular irritation that would preclude contact lens fitting;
Had eye surgery or any systemic or ocular medication within 12 weeks immediately prior to enrolment for this trial;
Undergone corneal refractive surgery;
Worn RGP’s or orthokeratology lenses within the previous two weeks;
Contraindications to hydrogel contact lens wear;
Contraindication / allergy to tobramycin;
Be currently enrolled in another clinical trial or have participated in a clinical trial within the previous two weeks.
Females are excluded from the trial

Study & Design

• Study Type: Interventional
• Study Design: Not specified