Comfort & Cleaning Evaluation of Multipurpose Solutions in NCT00519948

Updated 06/21/2024

Clinical Trial Details — Status: Completed

Administrative data
NCT number	NCT00519948
Other study ID #	5320
Secondary ID
Status	Completed
Phase	Phase 4
First received	August 21, 2007
Last updated	June 16, 2008
Est. completion date	June 2008

Study information
Verified date	June 2008
Source	Innovative Medical
Contact	n/a
Is FDA regulated	No
Health authority	United States: Institutional Review Board
Study type	Interventional

Clinical Trial Summary

To compare patient comfort and overall lens cleanliness with consecutive use of two multipurpose lens solutions.

Recruitment information / eligibility
Status	Completed
Enrollment	20
Est. completion date	June 2008
Est. primary completion date	June 2008
Accepts healthy volunteers
Gender	Both
Age group	18 Years and older
Eligibility	Inclusion Criteria: 1. Patients 18 yrs or older 2. Males or females 3. Any race or ethnic background 4. CL patients using Opti-Free Express no-rub MPS currently 5. Patients using Focus night and day Lenses Exclusion Criteria: 1. Corneal refractive surgery within 6 months of this study. 2. Corneal ectasia. 3. Current use of Restasis

Study Design

Intervention Model: Crossover Assignment, Masking: Open Label

Related Conditions & MeSH terms

Intervention

Drug:
• new MPS, opti-free express no rub MPS

Locations
Country	Name	City	State
United States	Eyeworks Group	Fort Worth	Texas

Sponsors *(1)*
Lead Sponsor	Collaborator
Innovative Medical

Country where clinical trial is conducted

United States,

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