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Cycloplegic Delivery Investigation

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ClinicalTrials.gov Identifier: NCT00472524
Recruitment Status : Completed
First Posted : May 11, 2007
Last Update Posted : July 3, 2008
Sponsor:
Information provided by:
Ohio State University

Brief Summary:
The goal of this study is to compare the effectiveness of the administration of sequential drops, a combination drop and a combination spray for producing mydriasis and cycloplegia.

Condition or disease Intervention/treatment Phase
Healthy Procedure: Mydriasis/cycloplegia via different modes of administration Not Applicable

Study Type : Interventional  (Clinical Trial)
Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic




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Ages Eligible for Study:   8 Years to 30 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • patients ages 8 to 30 with best corrected acuity of 20/30 or better in both eyes at distance and near will be recruited.

Exclusion Criteria:

  • vision not correctable to 20/30 or better

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00472524


Sponsors and Collaborators
Ohio State University
Investigators
Principal Investigator: Marjean Kulp, OD, MS Ohio State University

ClinicalTrials.gov Identifier: NCT00472524     History of Changes
Other Study ID Numbers: 2003H0072
First Posted: May 11, 2007    Key Record Dates
Last Update Posted: July 3, 2008
Last Verified: July 2008