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Single Dose of 1% Tropicamide and 10% Phenylephrine for Pupillary Dilation - Article


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Phenylephrine and Guaifenesin Capsules

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Clinical Trial: Single Dose of 1% Tropicamide and 10% Phenylephrine for Pupillary Dilation

This study has been completed.

Sponsored by: Khon Kaen University
Information provided by: Khon Kaen University
ClinicalTrials.gov Identifier: NCT00120432

Purpose

The purpose of this study is to compare the efficacy on pupillary dilation between the single dose versus the three doses of 1% tropicamide with 10% phenylephrine for complete ocular examination.
Condition Intervention Phase
Eye Diseases
 Drug: 1% tropicamide and 10% phenylephrine
Phase III

MedlinePlus related topics:  Eye Diseases

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study

Further Study Details: 
Primary Outcomes: horizontal pupil diameter
Secondary Outcomes: systolic blood pressure; diastolic blood pressure; heart rate; adverse drug reaction; time to pupil dilation greater than 6 mm
Expected Total Enrollment:  80

Study start: December 2004;  Study completion: July 2005
Last follow-up: June 2005;  Data entry closure: June 2005

To the best of the authors'''' knowledge, there have been no clinical trials using an appropriate regimen for pupillary dilation up until now. Therefore, the authors were interested to find out the most appropriate regimen for complete ocular examination, based on the finding that a pupil diameter of 6 mm or greater is adequate for indirect ophthalmoscopy. The authors hypothesize that a single dose of 1% tropicamide and 10% phenylephrine is adequate to complete the job and are conducting this prospective randomized clinical controlled trial to prove the hypothesis.

Eligibility

Ages Eligible for Study:  20 Years   -   80 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • aged between 20 and 80 years old
  • dark iris
  • require binocular indirect ophthalmoscopy for complete ocular examination
  • signed written consent forms

Exclusion Criteria:

  • history of ocular trauma
  • history of intraocular surgery
  • history of laser treatment
  • previous eye drop instillation that may affect pupillary dilation
  • ocular diseases that may affect pupil size such as Horner’s syndrome, Adies’ pupil, glaucoma and uveitis
  • history of diabetes mellitus, severe hypertension and cardiovascular diseases

Location Information


Thailand
      Srinagarind Hospital, Khon Kaen,  40002,  Thailand

Study chairs or principal investigators

Yosanan Yospaiboon, M.D.,  Principal Investigator,  Faculty of Medicine, Khon Kaen University   

More Information

Study ID Numbers:  HE461104
Last Updated:  July 18, 2005
Record first received:  July 15, 2005
ClinicalTrials.gov Identifier:  NCT00120432
Health Authority: Thailand: Khon Kaen University Ethics Committee for Human Research
ClinicalTrials.gov processed this record on 2005-08-02

Resources



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November 27, 2009



Page Updated: June 1, 2005
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