Actively Recruiting
Does Topical Ophthalmic Proparacaine 0.5% Prior to Probing and Irrigation Decrease Pain?
Led by Louisiana State University Health Sciences Center in New Orleans · Updated on 2022-12-23
145
Participants Needed
1
Research Sites
135 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Purpose: It is unknown whether instillation of a drop of anesthetic ophthalmic solution into the eye such as proparacaine hydrochloride 0.5% prior to probing and irrigation of the tear duct (lacrimal drainage) system improves participant comfort during the procedure. To date, there have been no formal studies evaluating the possible benefit of this pretreatment. Methods: Participants 18 years and older who present to the Louisiana State University or associated outpatient ophthalmology clinic(s) with a complaint of epiphora (excessive tearing) who necessitate bilateral lower lid probing and irrigation of the lacrimal drainage system will be enrolled in the study. One eye will be randomized to receive a drop of the anesthetic Proparacaine hydrochloride 0.5% and the other eye will receive a control drop of Balanced Salt Solution (BSS). Probing and irrigation will then be performed in the usual fashion. The participant will then be questioned via survey on a pain scale of 1-5 as to the amount of subjective pain experienced on each side during the procedure. Expected Results: Investigators expect participants will experience statistically significantly less pain in eyes that have received a drop of Proparacaine hydrochloride 0.5% prior to performance of probing and irrigation compared to the eyes which have received the control drop.
CONDITIONS
Official Title
Does Topical Ophthalmic Proparacaine 0.5% Prior to Probing and Irrigation Decrease Pain?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Signs and symptoms of excessive tearing (epiphora) requiring diagnostic probing and irrigation of both lower eyelid tear ducts
- Presenting for evaluation at Louisiana State University Health Sciences Center or affiliated clinics
You will not qualify if you...
- Known allergy to topical proparacaine hydrochloride
- Previous scarring, surgery, or radiation affecting the nasolacrimal drainage system
- Presence of blockage or reflux detected during probing and irrigation on either side
- Cognitive impairment affecting participation
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Louisiana State University Health Sciences Center
New Orleans, Louisiana, United States, 70112
Actively Recruiting
Research Team
A
Austin M Pharo, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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