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Timolol Option for Ulcerated Hemangiomas (TOUCH Trial) (TOUCH)

Primary Purpose

Infantile Hemangiomas

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Timolol 0.5% Gel Forming Solution (GFS)
Mupirocin 2% Ointment
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infantile Hemangiomas focused on measuring Hemangioma, Infantile Hemangioma, Ulcerated Hemangioma, Timolol, Beta blocker, Vascular anomaly

Eligibility Criteria

1 Month - 8 Months (Child)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Timolol 0.5% Gel Forming Solution (GFS)

Mupirocin 2% ointment

Arm Description

Half of enrolled subjects will receive topical Timolol

Half of enrolled subjects will receive Mupirocin

Outcomes

Primary Outcome Measures

Time to Wound Re-epithelization

Secondary Outcome Measures

Reduction in Ulcer Surface Area and Depth
Investigator's Global Evaluation of Disease
A scoring system developed to measure clinical improvement of ulcerated hemangioma.
Timolol Serum Level
Evaluate number of participants with changes in Glucose levels after drug is applied
Glucose monitoring will be performed for patients receiving Timolol 0.5% GFS before and 1 hour after drug is applied in clinic. Glucose values < 60 mg/dL will be considered significant. 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.
Evaluate number of participants with evidence of changes in blood pressure following administration of Timolol 0.5% GFS
Blood pressure monitoring will be performed for patients receiving Timolol 0.5% GFS before and 1 hour after drug is applied in clinic. Blood pressure values < 3rd percentile (systolic or diastolic) will be considered significant for hypotension. 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.
Pain scores (presence or absence) on the Wong-Baker faces scale
Investigators will question caregivers about common complications of ulcerated hemangiomas (pain, infection, bleeding) at each visit throughout the study. Pain will be assessed using the Wong-Baker faces scale. 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.
Number of participants with presence or absence of Infection
Investigators will question caregivers about common complications of ulcerated hemangiomas (pain, infection, bleeding) at each visit throughout the study. Infection will be clinically assessed by presence of drainage or exudate, and/or culture positivity. 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.
Number of participants with presence (or absence) of active bleeding
Investigators will question caregivers about common complications of ulcerated hemangiomas (pain, infection, bleeding) at each visit throughout the study. Infection will be clinically assessed by presence of active bleeding. 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.
Evaluate number of participants with changes in Heart Rate after drug is applied
Glucose and vital sign monitoring will be performed for patients receiving Timolol 0.5% GFS before and 1 hour after drug is applied in clinic. Heart rate values < 3rd percentile will be considered significant and indicative of bradycardia. 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.

Full Information

First Posted
March 10, 2011
Last Updated
January 16, 2014
Sponsor
Children's Hospital of Philadelphia
Collaborators
Society for Pediatric Dermatology
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1. Study Identification

Unique Protocol Identification Number
NCT01408056
Brief Title
Timolol Option for Ulcerated Hemangiomas (TOUCH Trial)
Acronym
TOUCH
Official Title
The Efficacy of Timolol 0.5% Gel Forming Solution for the Treatment of Ulcerated Hemangiomas
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Withdrawn
Why Stopped
Difficulty with recruitment
Study Start Date
February 2011 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital of Philadelphia
Collaborators
Society for Pediatric Dermatology

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infantile Hemangiomas
Keywords
Hemangioma, Infantile Hemangioma, Ulcerated Hemangioma, Timolol, Beta blocker, Vascular anomaly

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Timolol 0.5% Gel Forming Solution (GFS)
Arm Type
Experimental
Arm Description
Half of enrolled subjects will receive topical Timolol
Arm Title
Mupirocin 2% ointment
Arm Type
Active Comparator
Arm Description
Half of enrolled subjects will receive Mupirocin
Intervention Type
Drug
Intervention Name(s)
Timolol 0.5% Gel Forming Solution (GFS)
Other Intervention Name(s)
Timolol 0.5% topical
Intervention Description
Dose-based escalation schedule for topical application: 4-8 kg: Day 0-7: 1 drop every other day; Day 7-14: 1 drop daily; Day 14 - Day 60: 1 drop twice per day 8-12 kg: Day 07: 1 drop daily; Day 7-14: 1 drop twice per day; Day 14 - Day 60: 2 drops twice per day
Intervention Type
Drug
Intervention Name(s)
Mupirocin 2% Ointment
Other Intervention Name(s)
Mupirocin
Intervention Description
Topical application twice per day for 60 days
Primary Outcome Measure Information:
Title
Time to Wound Re-epithelization
Time Frame
At 3 months
Secondary Outcome Measure Information:
Title
Reduction in Ulcer Surface Area and Depth
Time Frame
At 3 months
Title
Investigator's Global Evaluation of Disease
Description
A scoring system developed to measure clinical improvement of ulcerated hemangioma.
Time Frame
At 3 months
Title
Timolol Serum Level
Time Frame
Measured at 1 month into therapy
Title
Evaluate number of participants with changes in Glucose levels after drug is applied
Description
Glucose monitoring will be performed for patients receiving Timolol 0.5% GFS before and 1 hour after drug is applied in clinic. Glucose values < 60 mg/dL will be considered significant. 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.
Time Frame
Baseline, day 7, day 14
Title
Evaluate number of participants with evidence of changes in blood pressure following administration of Timolol 0.5% GFS
Description
Blood pressure monitoring will be performed for patients receiving Timolol 0.5% GFS before and 1 hour after drug is applied in clinic. Blood pressure values < 3rd percentile (systolic or diastolic) will be considered significant for hypotension. 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.
Time Frame
Baseline, day 7, day 14
Title
Pain scores (presence or absence) on the Wong-Baker faces scale
Description
Investigators will question caregivers about common complications of ulcerated hemangiomas (pain, infection, bleeding) at each visit throughout the study. Pain will be assessed using the Wong-Baker faces scale. 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.
Time Frame
Baseline, day 7, day 14, 1 month, 2 months
Title
Number of participants with presence or absence of Infection
Description
Investigators will question caregivers about common complications of ulcerated hemangiomas (pain, infection, bleeding) at each visit throughout the study. Infection will be clinically assessed by presence of drainage or exudate, and/or culture positivity. 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.
Time Frame
Baseline, day 7, day 14, 1 month, 2 months
Title
Number of participants with presence (or absence) of active bleeding
Description
Investigators will question caregivers about common complications of ulcerated hemangiomas (pain, infection, bleeding) at each visit throughout the study. Infection will be clinically assessed by presence of active bleeding. 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.
Time Frame
Baseline, day 7, day 14, 1 month, 2 months
Title
Evaluate number of participants with changes in Heart Rate after drug is applied
Description
Glucose and vital sign monitoring will be performed for patients receiving Timolol 0.5% GFS before and 1 hour after drug is applied in clinic. Heart rate values < 3rd percentile will be considered significant and indicative of bradycardia. 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.
Time Frame
Baseline, day 7, day 14

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
8 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Albert C. Yan, MD
Organizational Affiliation
Children's Hospital of Philadelphia, Chair of Pediatric Dermatology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Vikash S. Oza, MD
Organizational Affiliation
Children's Hospital of Philadelphia, Attending Physician
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patrick McMahon, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20479314
Citation
Pope E, Chakkittakandiyil A. Topical timolol gel for infantile hemangiomas: a pilot study. Arch Dermatol. 2010 May;146(5):564-5. doi: 10.1001/archdermatol.2010.67. No abstract available.
Results Reference
background
PubMed Identifier
19143471
Citation
Sivamani RK, Pullar CE, Manabat-Hidalgo CG, Rocke DM, Carlsen RC, Greenhalgh DG, Isseroff RR. Stress-mediated increases in systemic and local epinephrine impair skin wound healing: potential new indication for beta blockers. PLoS Med. 2009 Jan 13;6(1):e12. doi: 10.1371/journal.pmed.1000012.
Results Reference
background
PubMed Identifier
19706583
Citation
Sans V, de la Roque ED, Berge J, Grenier N, Boralevi F, Mazereeuw-Hautier J, Lipsker D, Dupuis E, Ezzedine K, Vergnes P, Taieb A, Leaute-Labreze C. Propranolol for severe infantile hemangiomas: follow-up report. Pediatrics. 2009 Sep;124(3):e423-31. doi: 10.1542/peds.2008-3458. Epub 2009 Aug 10.
Results Reference
background
PubMed Identifier
21158749
Citation
Khunger N, Pahwa M. Dramatic response to topical timolol lotion of a large hemifacial infantile haemangioma associated with PHACE syndrome. Br J Dermatol. 2011 Apr;164(4):886-8. doi: 10.1111/j.1365-2133.2010.10177.x. No abstract available.
Results Reference
background
PubMed Identifier
18035154
Citation
Chamlin SL, Haggstrom AN, Drolet BA, Baselga E, Frieden IJ, Garzon MC, Horii KA, Lucky AW, Metry DW, Newell B, Nopper AJ, Mancini AJ. Multicenter prospective study of ulcerated hemangiomas. J Pediatr. 2007 Dec;151(6):684-9, 689.e1. doi: 10.1016/j.jpeds.2007.04.055. Epub 2007 Aug 24. Erratum In: J Pediatr. 2008 Apr;152(4):597.
Results Reference
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Timolol Option for Ulcerated Hemangiomas (TOUCH Trial)

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