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NCT00493662 Clinical Trial

Cross-Over Evaluation of Two Lubricating Eye Drops

Dry Eye Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00493662
Other study ID # 5310
Secondary ID
Status Completed
Phase Phase 4
First received June 26, 2007
Last updated January 11, 2008

Study information
Verified date January 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 evaluate the efficacy of two lubricating eye drops for the treatment of dry eye signs and symptoms.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
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. Patients with present ocular surface discomfort and a SESoD score of at least 2

Exclusion Criteria:

1. Corneal refractive surgery within 6 months of this study.

2. Contact lens use on day of examination.

3. Corneal ectasia.

4. Current use of Restasis

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind

Related Conditions & MeSH terms

Intervention

Drug:
• Polyethylene Glycol 400 0.4%

• Propylene Glycol 0.3%

• 0.15% sodium Hyaluronate

• sodium chloride

• sodium phosphate monobasic

Locations
Country Name City State
United States Hazleton Eye Specialists Hazleton Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
Innovative Medical

Country where clinical trial is conducted

United States, 

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