Cycloplegic Delivery Investigation

This study has been completed.
Sponsor:
Information provided by:
Ohio State University
ClinicalTrials.gov Identifier:
NCT00472524
First received: May 9, 2007
Last updated: July 1, 2008
Last verified: July 2008

May 9, 2007
July 1, 2008
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Complete list of historical versions of study NCT00472524 on ClinicalTrials.gov Archive Site
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Cycloplegic Delivery Investigation
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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.

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Interventional
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Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Healthy
Procedure: Mydriasis/cycloplegia via different modes of administration
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
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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
Both
8 Years to 30 Years
Yes
Contact information is only displayed when the study is recruiting subjects
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NCT00472524
2003H0072
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Ohio State University
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Principal Investigator: Marjean Kulp, OD, MS Ohio State University
Ohio State University
July 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP