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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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