Comfort Evaluation of a New MPS vs. Replenish in Contact Lens Patients
Sponsor
Innovative Medical (Industry)
Overall Status
Completed
CT.gov ID
NCT00518700
Collaborator
(none)
24
1
Study Details
Study Description
Brief Summary
To compare corneal staining after contact lens instillation with a new MPS vs. RepleniSH
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Study Design
Study Type:
Interventional
Actual Enrollment
:
24 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Investigator)
Actual Primary Completion Date
:
Apr 1, 2008
Actual Study Completion Date
:
Apr 1, 2008
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 MPS products currently
-
Patients using Contact Lenses habitually (at least 1 month)
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 | Private Practice | Azusa | California | United States | 91702 |
Sponsors and Collaborators
- Innovative Medical
Investigators
- Principal Investigator: Milton Hom, OD, FAAO, Private Practice
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00518700
Other Study ID Numbers:
- 5321
First Posted:
Aug 21, 2007
Last Update Posted:
Apr 24, 2008
Last Verified:
Apr 1, 2008