Cross-Over Evaluation of Two Lubricating Eye Drops
This study has been completed.
Sponsor:
Innovative Medical
Information provided by:
Innovative Medical
ClinicalTrials.gov Identifier:
NCT00493662
First received: June 26, 2007
Last updated: January 11, 2008
Last verified: January 2008
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
To evaluate the efficacy of two lubricating eye drops for the treatment of dry eye signs and symptoms.
| Condition | Intervention | Phase |
|---|---|---|
|
Dry Eye |
Drug: Polyethylene Glycol 400 0.4% Drug: Propylene Glycol 0.3% Drug: 0.15% sodium Hyaluronate Drug: sodium chloride Drug: sodium phosphate monobasic |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Single Blind |
Resource links provided by NLM:
Drug Information available for:
Propylene glycol
Sodium phosphate monobasic
Sodium phosphate
Sodium chloride
Chlorine
Polyethylene
Hyaluronic Acid
Hyaluronate Sodium
Sodium phosphate, dibasic
Polyethylene glycol
U.S. FDA Resources
Further study details as provided by Innovative Medical:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
Criteria
Inclusion Criteria:
- Patients 18 yrs or older
- Males or females
- Any race or ethnic background
- Patients with present ocular surface discomfort and a SESoD score of at least 2
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
Please refer to this study by its ClinicalTrials.gov identifier: NCT00493662
Locations
| United States, Pennsylvania | |
| Hazleton Eye Specialists | |
| Hazleton, Pennsylvania, United States, 18202 | |
Sponsors and Collaborators
Innovative Medical
Investigators
| Principal Investigator: | Tom Kislan, OD | Hazleton Eye Specialists |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00493662 History of Changes |
| Other Study ID Numbers: | 5310 |
| Study First Received: | June 26, 2007 |
| Last Updated: | January 11, 2008 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Hyaluronic Acid Sodium phosphate Adjuvants, Immunologic Immunologic Factors Physiological Effects of Drugs |
Pharmacologic Actions Cathartics Gastrointestinal Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 19, 2013