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Propranolol in Capillary Hemangiomas (HEMANGIOMA)

Primary Purpose

Hemangioma, Capillary

Status
Terminated
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
propranolol treatment
placebo treatment
Sponsored by
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemangioma, Capillary focused on measuring infantile capillary hemangiomas, propranolol, ultrasonography

Eligibility Criteria

undefined - 4 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infant aged less than 4 months
  • Infant with one or more hemangiomas sized more than 1 cm diameter
  • Infant not threatening for vital or functional structure and for which no treatment would be proposed
  • Informed consent
  • Patient with social insurance.

Exclusion Criteria:

  • Alarming hemangioma (s) (complicated forms or localization at risk)
  • Cardiac pathology (cardiac malformation, heart failure, cardiac arrhythmias, pulmonary hypertension)
  • Asthma
  • Bronchopulmonary dysplasia
  • Bronchiolitis
  • Raynaud syndrome
  • Phéochromocytoma
  • Development of serious form of hemangioma (bleeding, necrosis, ulceration, infection, respiratory distress) requiring standard treatment

Sites / Locations

  • Dermatologie Pédiatrique

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

2

1

Arm Description

30-days placebo treatment

30-days propranolol treatment

Outcomes

Primary Outcome Measures

Proportion of hemangioma thickness variation measured by ultrasonography from the basal state between the two groups after 1 month-treatment.

Secondary Outcome Measures

Proportion of hemangioma size variation measured clinically and with photography from the basal state between the two groups after 1 month-treatment.
Observance

Full Information

First Posted
August 28, 2008
Last Updated
July 18, 2012
Sponsor
University Hospital, Bordeaux
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1. Study Identification

Unique Protocol Identification Number
NCT00744185
Brief Title
Propranolol in Capillary Hemangiomas
Acronym
HEMANGIOMA
Official Title
Double Blind, Randomised, Placebo-controlled Study of Propranolol in Infantile Capillary Hemangiomas
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Terminated
Why Stopped
Study halted prematurely due to some difficulties in recruitment of patients
Study Start Date
October 2008 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
April 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators observed that Propranolol, a beta-blocker commonly used in children was efficient to control the growth of alarming hemangiomas of the face. The primary objective of this study is to determine the efficiency of 1 month-early treatment of propranolol in infants aged less than 4 months affected by an hemangioma without any consequences on vital or functional structure and not justifying corticosteroids. The secondary objectives are: the kinetic of the hemangioma evolution in infants treated by propranolol Observance Safety
Detailed Description
Infantile hemangiomas are frequent vascular tumors (4 à 10 % of the neonates) and correspond to 100 new cases per year in dermatology consultation of the CHU of Bordeaux. Hemangiomas have a characteristic clinical course marked by early proliferation during 3 to 12 months followed by slow and spontaneous involution from 3 to 7 years. Occasionally, as well as esthetical damages, hemangiomas may impair vital structures, ulcerate, bleed, or cause high-output cardiac failure or significant structural abnormalities. Standard treatments (corticotherapy, interferon, vincristine…) lead to a stagnation of hemangiomas in some cases, but with frequent side effects. We observed that Propranolol, a beta-blocker usually used in neonates could lead to a decreased in volume of serious haemangiomas of the face (article published in New England Journal of Medicine). In this study, we proposed to determine the efficiency of 1 month-early treatment of propranolol in neonates aged less than 4 months affected by non alarming hemangioma and not justifying corticotherapy. This is a double blind randomized placebo controlled study of propranolol. Infants will be recruited from the dermatology consultation of CHU Bordeaux. After verification of eligibility criteria and informed consent of legal surrogates, infants will be randomized to receive either propranolol or either placebo. The infants will be observed during 1 month according to the following visits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemangioma, Capillary
Keywords
infantile capillary hemangiomas, propranolol, ultrasonography

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
2
Arm Type
Placebo Comparator
Arm Description
30-days placebo treatment
Arm Title
1
Arm Type
Experimental
Arm Description
30-days propranolol treatment
Intervention Type
Drug
Intervention Name(s)
propranolol treatment
Intervention Description
30 days-propranolol treatment : 3 mg/kg 15 days + 4 mg/kg 15 days
Intervention Type
Drug
Intervention Name(s)
placebo treatment
Intervention Description
30 days-placebo treatment : 3 mg/kg 15 days + 4 mg/kg 15 days
Primary Outcome Measure Information:
Title
Proportion of hemangioma thickness variation measured by ultrasonography from the basal state between the two groups after 1 month-treatment.
Time Frame
30 days treatment
Secondary Outcome Measure Information:
Title
Proportion of hemangioma size variation measured clinically and with photography from the basal state between the two groups after 1 month-treatment.
Time Frame
30 days-treatment
Title
Observance
Time Frame
30 days-treatment

10. Eligibility

Sex
All
Maximum Age & Unit of Time
4 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infant aged less than 4 months Infant with one or more hemangiomas sized more than 1 cm diameter Infant not threatening for vital or functional structure and for which no treatment would be proposed Informed consent Patient with social insurance. Exclusion Criteria: Alarming hemangioma (s) (complicated forms or localization at risk) Cardiac pathology (cardiac malformation, heart failure, cardiac arrhythmias, pulmonary hypertension) Asthma Bronchopulmonary dysplasia Bronchiolitis Raynaud syndrome Phéochromocytoma Development of serious form of hemangioma (bleeding, necrosis, ulceration, infection, respiratory distress) requiring standard treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicholas Moore, Professor
Organizational Affiliation
University Hospital Bordeaux, France
Official's Role
Study Chair
Facility Information:
Facility Name
Dermatologie Pédiatrique
City
Bordeaux
ZIP/Postal Code
33 076
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
18550886
Citation
Leaute-Labreze C, Dumas de la Roque E, Hubiche T, Boralevi F, Thambo JB, Taieb A. Propranolol for severe hemangiomas of infancy. N Engl J Med. 2008 Jun 12;358(24):2649-51. doi: 10.1056/NEJMc0708819. No abstract available.
Results Reference
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PubMed Identifier
14583354
Citation
Tortoriello TA, Snyder CS, Smith EO, Fenrich AL Jr, Friedman RA, Kertesz NJ. Frequency of recurrence among infants with supraventricular tachycardia and comparison of recurrence rates among those with and without preexcitation and among those with and without response to digoxin and/or propranolol therapy. Am J Cardiol. 2003 Nov 1;92(9):1045-9. doi: 10.1016/j.amjcard.2003.06.002.
Results Reference
background
PubMed Identifier
15321698
Citation
Villain E, Denjoy I, Lupoglazoff JM, Guicheney P, Hainque B, Lucet V, Bonnet D. Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome. Eur Heart J. 2004 Aug;25(16):1405-11. doi: 10.1016/j.ehj.2004.06.016.
Results Reference
background
PubMed Identifier
12661740
Citation
Kilian K. Hypertension in neonates causes and treatments. J Perinat Neonatal Nurs. 2003 Jan-Mar;17(1):65-74; quiz 75-6. doi: 10.1097/00005237-200301000-00006.
Results Reference
background
PubMed Identifier
9527943
Citation
Fritz KI, Bhat AM. Effect of beta-blockade on symptomatic dexamethasone-induced hypertrophic obstructive cardiomyopathy in premature infants: three case reports and literature review. J Perinatol. 1998 Jan-Feb;18(1):38-44.
Results Reference
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Propranolol in Capillary Hemangiomas

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