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Efficacy and Safety of Propranolol Versus Acebutolol on the Proliferative Phase of Infantile Hemangioma

Efficacy and Safety of Propranolol Versus Acebutolol on the Proliferative Phase of Infantile Hemangioma

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01743885
Enrollment
55
Registered
2012-12-06
Start date
2012-11-30
Completion date
2015-06-30
Last updated
2016-06-01

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

Conditions

Hemangioma

Keywords

Hemangioma, Beta-blocker, Acebutolol, Propranolol, Randomized controlled trial, Infants

Brief summary

There is no effective treatment for hemangioma regardless of immediate severity. That is in this respect a orphan disease. These hemangiomas, sometimes large, will have a phase of proliferation of several months (very scary for parents) and regression over several years. The natural history is peppered with local complications (ulcers) and aesthetic and psychological sequelae (sometimes major for the child and the family). The effects of acebutolol and propranolol on the proliferative hemangiomas were discovered accidentally by two French teams (Montpellier for acebutolol and Bordeaux for propranolol). Acebutolol and propranolol have been used for many years for the treatment of hypertension and congenital heart disease, including infants, with few side effects. The effects of acebutolol and propranolol were immediately visible with reduced volume and skin whitening of the hemangioma. In a preliminary study, acebutolol was administered to 20 patients in Montpellier with big regression of hemangiomas. The aim of the study was to compare the clinical efficacy of acebutolol (10mg/Kg/jour) and propranolol (3mg/Kg/j) on the proliferative phase of infantile hemangioma in infants.

Interventions

10 mg/kg/jour in 2 doses during 90 days after gradual increase of doses in the first week

3 mg/kg/jour in 3 doses during 90 days after gradual increase of doses in the first week

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
No minimum to 6 Months
Healthy volunteers
No

Inclusion criteria

* Infants under 6 months * Presenting a hemangioma with the following characteristics: * subcutaneous and / or cutaneous * minimum diameter of 1.5cm on face, 5cm outside face and 3cm if it is ulcerated. * without functional impairment requiring treatment or vital corticosteroid * Consent of both parents (or the person having parental authority in families) * Which at least one parent is a beneficiary of a social security system.

Exclusion criteria

* Indication of treatment with corticosteroids for an indication other than hemangioma * Indication of treatment with beta-blocker for another indication that the hemangioma * Infant presenting cons-indications for the administration of acebutolol or propranolol: * Asthma and chronic obstructive pulmonary disease in their severe forms. * Heart failure controlled by treatment. * Cardiogenic shock * Prinzmetal Angina * Bradycardia (\<80 beats / min at rest the first month \<70/minute from 1 to 6 month). * Raynaud's phenomenon and peripheral arterial disorders in their severe forms. * Pheochromocytoma untreated. * Low blood pressure (blood pressure \<60/30 mmHg before 6 months) * Hypersensitivity to acebutolol or propranolol * History of anaphylactic reaction. * Treatment with amiodarone and / or calcium channel blockers. * Congenital heart disease outside inter auricular communication (CIA) or inter ventricular communication (CIV) insignificant

Design outcomes

Primary

MeasureTime frameDescription
Hemangioma size3 monthsIt will be evaluated using a VAS (visual analogue scale) on a series of photos at Day 0, Day 30 and Day 90

Secondary

MeasureTime frameDescription
Tolerance of treatment3 monthsAll adverse events are collected at each visited
Proportion of patients requiring treatment with corticosteroids because of the evolution of a 'serious' hemangioma3 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026