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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00120432
Other study ID # HE461104
Secondary ID
Status Completed
Phase Phase 3
First received July 11, 2005
Last updated March 7, 2012
Start date December 2004
Est. completion date June 2005

Study information

Verified date March 2012
Source Khon Kaen University
Contact n/a
Is FDA regulated No
Health authority Thailand: Khon Kaen University Ethics Committee for Human Research
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date June 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
1% tropicamide and 10% phenylephrine
single dose vs three doses of 1%tropicamide and 10%phenylephrine

Locations

Country Name City State
Thailand Srinagarind Hospital Khon Kaen

Sponsors (1)

Lead Sponsor Collaborator
Khon Kaen University

Country where clinical trial is conducted

Thailand, 

References & Publications (1)

Ratanapakorn T, Yospaiboon Y, Chaisrisawadsuk N. Single dose of 1% tropicamide and 10% phenylephrine for pupil dilation. J Med Assoc Thai. 2006 Nov;89(11):1934-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary horizontal pupil diameter 30 min No
Secondary systolic blood pressure 30 min Yes
Secondary diastolic blood pressure 30 min Yes
Secondary heart rate 30 min Yes
Secondary adverse drug reaction 30 min Yes
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