Post-market clinical follow-up for stenfilcon A sphere and toric lenses

Not Applicable

• Conditions: Myopia, astigmatism, hyperopia; Eye Diseases

• Registration Number: ISRCTN61640561
• Lead Sponsor: CooperVision

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-03-26
• Last Update Posted: 2 September 2024
• Study Completion: 2024-12-31

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

1. Aged 8 to 75 years old (inclusive)
2. Current wearer of the Stenfilcon A Sphere or Toric contact lens

Exclusion Criteria

1. Participation in a contact lens or contact lens care product clinical trial within the previous 30 days

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Visual performance measured using a visual acuity chart at the single study visit<br>2. Incidence of contact lens-related adverse events measured using a report of contact lens related adverse events in the past 12 months at the single study visit

Secondary Outcome Measures

Name	Time	Method
There are no secondary outcome measures