Clinical Trials Directory

Trials / Completed

CompletedNCT01282541

Determination of the Optimum Delivery Route for Botulinum Toxin A in Patients With Epiphora

Determination of the Optimum Delivery Route for the Intraglandular Administration of Botulinum Toxin A in Patients With Refractory Epiphora

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
26 (actual)
Sponsor
Merbs, Shannath, M.D., Ph.D. · Individual
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Epiphora or excessive tearing is a significant disability for many affected patients diminishing their quality of life. There is a growing consensus that injection of Botulinum Toxin A (BTX-A) into the lacrimal gland provides relief in patients with hyperlacrimation secondary to aberrant regeneration of the 7th nerve, and limited evidence that it might help to reduce normal tear production in patients with epiphora from anatomic or functional outflow obstructions. BTX-A has been injected both transconjunctivally into the palpebral lobe of the lacrimal gland and transcutaneously into the orbital lobe. Both delivery routes have been successful in symptom relief with minimal complications. However, the effectiveness of transconjunctival versus transcutaneous injections has not been systematically compared. Also, whether the incidence of side effects is related to the dosage, concentration, or location of injection is unknown and has also not been systematically studied. The investigators plan to conduct a randomized clinical trial in patients with functional tearing comparing the transcutaneous delivery route of BTX-A to the transconjunctival delivery route (the most common route described in the literature). The investigators will also compare the side effect profile of each delivery route.

Conditions

Interventions

TypeNameDescription
DRUGBotulinum Toxin Type A100 units/2ml 0.9% sodium chloride, 5 units delivered transconjunctivally into the palpebral lobe of the lacrimal gland once
DRUGBotulinum Toxin Type A100 units/2ml 0.9% sodium chloride, 5 units delivered transcutaneously into the orbital lobe of the lacrimal gland once

Timeline

Start date
2011-02-01
Primary completion
2012-09-01
Completion
2012-09-01
First posted
2011-01-25
Last updated
2012-09-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01282541. Inclusion in this directory is not an endorsement.