Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining
Sponsor
Innovative Medical (Industry)
Overall Status
Completed
CT.gov ID
NCT00483795
Collaborator
(none)
1
Study Details
Study Description
Brief Summary
To evaluate corneal staining after contact lens instillation with two different multi purpose solutions.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Study Design
Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
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
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Hazleton Eye Specialists | Hazleton | Pennsylvania | United States | 18202 |
Sponsors and Collaborators
- Innovative Medical
Investigators
- Principal Investigator: Thomas Kislan, OD, Hazleton Eye Specialists
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00483795
Other Study ID Numbers:
- 5308
First Posted:
Jun 7, 2007
Last Update Posted:
Jul 25, 2007
Last Verified:
Jul 1, 2007