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The purpose of this study is to determine the safety and efficiency of Propranolol as an initial treatment for pediatric hemangioma.
* Randomized (A group : propranolol, B group : prednisolone) * A group : 3 days admission and medication for 16 weeks * B group : medication for 16 weeks without admission * Hemangioma volume comparison by using MRI * other measurement and drug adverse reaction monitoring
Age
0 - 0 years
Sex
ALL
Healthy Volunteers
No
Seould National University Hospital
Seoul, South Korea
Start Date
June 1, 2013
Primary Completion Date
May 1, 2015
Completion Date
May 1, 2015
Last Updated
December 19, 2018
34
ACTUAL participants
Prednisolone
DRUG
Propranolol
DRUG
Lead Sponsor
Seoul National University Hospital
NCT07418294
NCT01873131
NCT01764529
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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