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Clinical Trials/TCTR20130325001
TCTR20130325001
Completed
Phase 3

A randomized comparative study of the efficacy on pupillary dilatation between separate bottles of dilating eye drops and a single-bottle eye drop mixture.

one0 sites28 target enrollmentMarch 25, 2013
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ConditionsPupillary dilatation&#45diclofenacphenylephrinetropicamidepupillary dilatationmydriatic

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Pupillary dilatation
Sponsor
one
Enrollment
28
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 25, 2013
End Date
March 12, 2014
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
one

Eligibility Criteria

Inclusion Criteria

  • •\- age 18 or older
  • •\- clear cornea (pupil can be easily measured)
  • •\- patients with hypertension must have resting BP not more than 160/95 mmHg
  • •\- patient receives studied eye drops in only 1 eye

Exclusion Criteria

  • •\- pupil distortion or any congenital anomaly of pupil (such as corectopia)
  • •\- untreated appositional angle or angle closure
  • •\- pregnancy
  • •\- allergic to any of the study drugs
  • •\- patient who cannot complete the study

Outcomes

Primary Outcomes

Not specified

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