Diurnal Variation in Tear Osmolarity
The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2011 by Ophthalmic Consultants of Long Island.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Ophthalmic Consultants of Long Island
Collaborator:
Allergan
Information provided by (Responsible Party):
Ophthalmic Consultants of Long Island
ClinicalTrials.gov Identifier:
NCT01321424
First received: March 21, 2011
Last updated: November 16, 2012
Last verified: March 2011
| Tracking Information | |||||||||
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| First Received Date ICMJE | March 21, 2011 | ||||||||
| Last Updated Date | November 16, 2012 | ||||||||
| Start Date ICMJE | March 2011 | ||||||||
| Estimated Primary Completion Date | January 2013 (final data collection date for primary outcome measure) | ||||||||
| Current Primary Outcome Measures ICMJE |
The measured difference in Tear Osmolarity during the course of the day to support clinical diagnosis and differentiate between aqueous-deficiency and meibomian gland disease. [ Time Frame: 1 Day (AM and PM Diurnal) ] [ Designated as safety issue: No ] | ||||||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||||||
| Change History | Complete list of historical versions of study NCT01321424 on ClinicalTrials.gov Archive Site | ||||||||
| Current Secondary Outcome Measures ICMJE |
Ocular Improvement [ Time Frame: 31 Days ] [ Designated as safety issue: No ] Improvement in Ocular Surface Disease Index, Best Corrected Visual Acuity, Uncorrected Visual Acuity, Slit Lamp Exam, Schirmer test, Lissamine green conjunctival staining, Fluorescein corneal staining and Tear Break Up Time |
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| Original Secondary Outcome Measures ICMJE |
Ocular Improvement [ Time Frame: 31 Days ] [ Designated as safety issue: No ] Improvement in OSDI, BCVA, UCVA, Slit Lamp Exam, Schirmer test, Lissamine green conjunctival staining, Fluorescein corneal staining and TBUT |
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| Current Other Outcome Measures ICMJE | Not Provided | ||||||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||||||
| Descriptive Information | |||||||||
| Brief Title ICMJE | Diurnal Variation in Tear Osmolarity | ||||||||
| Official Title ICMJE | Investigator Sponsored, Pilot Study to Assess the Diurnal Variation in Tear Osmolarity as a Predictor of Dry Eye Disease Etiology | ||||||||
| Brief Summary | The purpose of this study is to measure the change in Tear Osmolarity during the course of the day to support clinical diagnosis of aqueous deficiency or meibomian gland disease and differentiate between the two forms of dry eye. |
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| Detailed Description | The premise of this study is that dry eye disease, specifically tear osmolarity, changes during the course of the day based on the etiology of the dry eye and that aqueous-deficiency dry eye will worsen during the course of the day while meibomian gland deficiency will stabilize or possibly even improve during the course of the day. |
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| Study Type ICMJE | Observational | ||||||||
| Study Design ICMJE | Observational Model: Case Control Time Perspective: Cross-Sectional |
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| Target Follow-Up Duration | Not Provided | ||||||||
| Biospecimen | Not Provided | ||||||||
| Sampling Method | Non-Probability Sample | ||||||||
| Study Population | Primary care facility |
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| Condition ICMJE | Dry Eye Disease | ||||||||
| Intervention ICMJE | Not Provided | ||||||||
| Study Group/Cohort (s) |
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| Publications * | Not Provided | ||||||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status ICMJE | Recruiting | ||||||||
| Estimated Enrollment ICMJE | 60 | ||||||||
| Estimated Completion Date | January 2013 | ||||||||
| Estimated Primary Completion Date | January 2013 (final data collection date for primary outcome measure) | ||||||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||
| Ages | 18 Years and older | ||||||||
| Accepts Healthy Volunteers | Yes | ||||||||
| Contacts ICMJE |
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| Location Countries ICMJE | United States | ||||||||
| Administrative Information | |||||||||
| NCT Number ICMJE | NCT01321424 | ||||||||
| Other Study ID Numbers ICMJE | ALRGN01 | ||||||||
| Has Data Monitoring Committee | No | ||||||||
| Responsible Party | Ophthalmic Consultants of Long Island | ||||||||
| Study Sponsor ICMJE | Ophthalmic Consultants of Long Island | ||||||||
| Collaborators ICMJE | Allergan | ||||||||
| Investigators ICMJE |
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| Information Provided By | Ophthalmic Consultants of Long Island | ||||||||
| Verification Date | March 2011 | ||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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