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Targeted treatment of haemangioma with captopril

Pilot observational study to confirm the safety and efficacy of captopril in infants with problematic haemangioma

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000523909
Enrollment
8
Registered
2011-05-23
Start date
2010-10-29
Completion date
2010-11-05
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Strawberry birthmark (haemangioma) grows rapidly during infancy before gradually shrinking in later childhood. Rapidly growing haemangiomas can cause significant disfigurement and functional problems including threatened vision and life. The child affected by problematic growing haemangioma is considered for this study because we believe that Captopril, given in small doses could dramatically shrink the birthmark such that surgery and/or laser therapy would not be needed later on. Captopril has been used in infants and children with high blood pressure for many years. Our research suggests that Capopril will specifically target a particular type of cells in the haemangioma that are responsible for its rapid growth. In this study, we would start the child on small doses of Captopril, given by mouth. The medication is maintained until the birthmark is fully regressed or until 12 months of age

Interventions

Captopril oral solution titrated gradually to a maximum dose of 0.6mg/kg/day in 3 divided doses. With a starting dose of 0.15mg/kg/day in 3 divided doses until the child is 1 year of age.

Sponsors

Hutt Valley District Health Board
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
9 Weeks to 5 Years
Healthy volunteers
No

Inclusion criteria

: Infants and young children with growing problematic haemangiomas whose parents or guardians are willing, able, and competent to administer prescribed medications. (Problematic haemangiomas are defined in the literature as those that cause disruption to form/function of a child or that ulcerate)

Exclusion criteria

Parents and guardians who would not consent to participate in this study. Neonates Infants or children who have underlying cardiovascular disease

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026