Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining
July 23, 2007 updated by: Innovative Medical
To evaluate corneal staining after contact lens instillation with two different multi purpose solutions.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Pennsylvania
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Hazleton, Pennsylvania, United States, 18202
- Hazleton Eye Specialists
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients 18 yrs or older
- Males or females
- Any race or ethnic background
- CL patients using (multipurpose solutions) MPS
- Patients using Acuvue 2 lenses
Exclusion Criteria:
- Corneal refractive surgery within 6 months of this study.
- Contact lens use on day of examination.
- Corneal ectasia.
- Current use of Restasis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Thomas Kislan, OD, Hazleton Eye Specialists
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
June 1, 2007
First Submitted That Met QC Criteria
June 6, 2007
First Posted (Estimate)
June 7, 2007
Study Record Updates
Last Update Posted (Estimate)
July 25, 2007
Last Update Submitted That Met QC Criteria
July 23, 2007
Last Verified
July 1, 2007
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 5308
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.