Clinical Trials Directory

Trials / Completed

CompletedNCT01224847

Intravitreal Injection Anesthesia - Comparison of Different Topical Agents

Intravitreal Injection Anesthesia - Comparison of Different Topical Agents.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
92 (actual)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

Patients with neovascular age-related macular degeneration (AMD) scheduled to receive intravitreal (IVT) Ranibizumab injection will be randomized to receive one of three topical anesthetics: (1) tetracaine drop (gtt) + lidocaine pledget to the injection site for 10 seconds (2) tetracaine gtt alone and (3) cocaine gtt alone. A questionnaire will be conducted immediately after and 15 minutes after the injection, to assess for pain.

Detailed description

All patients scheduled to receive intravitreal Ranibizumab for the treatment of neovascular AMD will be evaluated for inclusion into the study. After a positive evaluation, the study will be explained to the patient, the Letter of Explanation reviewed with the patient and informed consent approved if patient agrees to participate. Demographic data of sex and age will be recorded. As well the number of previous intravitreal injections will be recorded ( none, 2 - 5 and \> 5 ). A nurse will then proceed to select an opaque envelope from a box of identical envelopes. The envelope will contain the topical anesthetic agent to be used. The randomization code linking each patient to their anesthetic will be stored in a secure location, and only accessed at the completion of the trial. The anesthetic procedure will be performed by someone other than the surgeon who will perform the IVT injection. After a minute of the anesthetic application, the surgeon, blinded to the anesthetic intervention, will perform the IVT injection of Ranibizumab. Immediately following the injection, a blinded observer will first explain the Pain Questionnaire, and then conduct it. Also at this time, the physician who performed the injection will complete the Wong-Baker Pain Questionnaire. The patient will then be asked to wait in a room for an additional 15 minutes, where the same observer will return and the Pain Questionnaire will be conducted a second time.

Conditions

Interventions

TypeNameDescription
DRUGTetracaine1 gtt
DRUGCocaine1 gtt
DRUGLidocaineLidocaine soaked pledget

Timeline

Start date
2009-10-01
Primary completion
2009-11-01
Completion
2009-11-01
First posted
2010-10-20
Last updated
2012-04-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01224847. Inclusion in this directory is not an endorsement.