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Study of INS365 Ophthalmic Solution in a Controlled Adverse Environment in Patients with Dry Eye



Study of INS365 Ophthalmic Solution in a Controlled Adverse Environment in Patients with Dry Eye

For Condition: Keratoconjunctivitis Sicca
Status: Completed
Sponsor(s): Inspire Pharmaceuticals ,
Synopsis: Comparative efficacy trial of INS365 Ophthalmic Solution and placebo in patients with dry eye.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: - have Non-Sjogren's associated dry eye disease with symptoms lasting greater than 6 months - had intermittent or regular artificial tear use within past 3 months - not had LASIK surgery - not had punctal occlusion or cauterization within last 3 months
Total Enrollment: 200

Location and Contact Information:

Ophthalmic Research Associates, Inc.
Andover,  Massachusetts,  01810
United States
 


Additional Information:
Study ID Numbers:
  03-108; 
Study Start Date: April 2002
Record last reviewed: August 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00037661

Other Keratoconjunctivitis Sicca Studies:
1. Study of INS365 Ophthalmic Solution in a Controlled Adverse Environment in Patients with Dry Eye

2. Six month clinical research study for patients with moderate or severe dry eye syndrome

3. Treatment of Dry Eye Syndrome with Cyclosporin A Eye Drops

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Study of INS365 Ophthalmic Solution in a Controlled Adverse Environment in Patients with Dry Eye

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