Timolol Option for Ulcerated Hemangiomas (TOUCH Trial)



Status:Completed
Conditions:Gastrointestinal, Hematology
Therapuetic Areas:Gastroenterology, Hematology
Healthy:No
Age Range:Any
Updated:1/1/2014
Start Date:February 2011
End Date:June 2013
Contact:Albert C. Yan, MD
Email:yana@email.chop.edu
Phone:215-590-2169

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The Efficacy of Timolol 0.5% Gel Forming Solution for the Treatment of Ulcerated Hemangiomas

The purpose of this study is to determine whether Timolol 0.5% Gel Forming Solution is safe
and effective in promoting wound healing of infantile ulcerated hemangiomas compared with
standard conservative management with topical antibiotic.

Ulceration is the most common complication associated with infantile hemangiomas. Ulceration
and the delay in wound healing places patients at risk for infection, bleeding, pain and
permanent scarring. Currently, the care of ulcerated hemangiomas is extremely difficult and
patients are often subject to multiple treatment modalities.

In the past two years, the leading advance in the treatment of hemangiomas has been the use
of the non-selective, oral beta-blocker propranolol to arrest growth and promote involution
of hemangiomas. Recent literature also suggests beta-blockers may have a role in helping
ulcerated wounds re-epithelialize.

The use of a topical non-selective beta-blocker on isolated ulcerated hemangiomas may
promote early healing and reduce the number of complications associated with ulceration.
Investigation is needed to explore the safety and tolerability of applying a topical
beta-blocker on an ulcerated hemangioma and whether topical beta-blockade may be more
efficacious than conservative care with topical antibiotics.

In this study, infants will be randomized to either receive a topical antibiotic (topical
mupirocin 2% ointment twice per day) or a topical beta-blocker (Timolol 0.5% Gel Forming
Solution) according to a dose-escalation schedule. Subjects will be seen in clinic on day 7,
day 14, 1 month and 2 months into therapy and 1 month after therapy is completed.
Photographs and safety and efficacy measurements will be taken at each visit to assess
response to therapy.

Inclusion Criteria:

- Infants weighing between 4-12kg

- Infants with corrected gestational age 44 weeks - 8 months of age

- Infant with an ulcerated hemangioma

- Informed consent

Exclusion Criteria:

- Ulceration larger than 16cm2

- Ulcerated hemangioma with active bleeding or infection at time of enrollment

- Disease threatening hemangioma meeting criteria for oral propranolol

- Previous treatment with topical/oral corticosteroid or propranolol

- Medical history of congenital heart disease with decreased cardiac output,
stroke/cerebral vasculopathy, active reactive airway disease or metabolic disorder

- History of an allergic reaction to Mupirocin or Timolol

- Currently taking medication that would interact with beta-blockers
We found this trial at
1
site
South 34th Street
Philadelphia, Pennsylvania 19104
 215-590-1000
Children's Hospital of Philadelphia Since its start in 1855 as the nation's first hospital devoted...
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Philadelphia, PA
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