None listed
Conditions
Brief summary
Pending
Interventions
Group A will receive amorphous gel and Group B will receive a Hydrocolloid
Sponsors
Royal Children's Hospital, Vic, Australia
Study design
Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)
Eligibility
Sex/Gender
All
Age
0 to 2 Years
Healthy volunteers
No
Inclusion criteria
Infants with ulcerated hemangioma of infancy between the age of 0-2 years.
Exclusion criteria
Infants who have known hypersensitivity to amorphous gel or a hydrocolloid.Infants with other serious medical conditions requiring therapy.If the ulcerated hemangioma is at a site where dressing cannot be applied.Infants where surgical removal of the ulcer is regarded as the best treatment.
Outcome results
None listed