Clinical Trials Directory

Trials / Terminated

TerminatedNCT00690222

Intracameral Mydriasis Versus Topical Mydriasis in Cataract Surgery

A Comparison of Intracameral Phenylephrine 2% and Tropicamide 0.2% With Topical Phenylephrine 2.5% and Tropicamide 1% for Pupillary Dilation During Cataract Surgery on Patients With and Without Pseudoexfoliation Syndrome.

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Nova Scotia Health Authority · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose is to determine if an intracameral solution of 0.2% tropicamide and 2% phenylephrine can dilate the pupil for cataract surgery as well as pre-operative topical 1% tropicamide and 5% phenylephrine. We will be looking at two separate groups of patients, those with and those without pseudoexfoliation syndrome. We will be looking at how each method affects the size of the pupil at the beginning and at the end of cataract surgery. In addittion, we will look at what effect the two different methods have on blood pressure and heart rate in the pre-operative, peri-operative and post-operative periods.

Conditions

Interventions

TypeNameDescription
PROCEDUREIntracameral injection of mydriatic agentA mixture of 0.2 % tropicamide and 2% phenylephrine will be injected into the anterior chamber at the beginning of surgery

Timeline

Start date
2008-03-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2008-06-04
Last updated
2015-03-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00690222. Inclusion in this directory is not an endorsement.