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Recolector de Ciencia Abierta, RECOLECTA
Bachelor thesis . 2014
License: CC BY NC ND
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Recolector de Ciencia Abierta, RECOLECTA
Bachelor thesis . 2014
License: CC BY NC ND
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
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Topical timolol treatment for infantile hemangiomas: a phase II multicentre randomized clinical trial

Authors: Seguí Olmedilla, Mireia;

Topical timolol treatment for infantile hemangiomas: a phase II multicentre randomized clinical trial

Abstract

Infantile hemangiomas (IHs) are common benign vascular tumours of infancy, although the best approach to their management remains unclear. IHs have a characteristic natural course, with a rapid proliferating phase followed by a spontaneous involuting phase, leaving in many cases residual lesions. The standard approach to uncomplicated IHs is “wait and see” but active intervention may be necessary since they can reach a considerable size and the aesthetic outcome is unpredictable. In addition, IHs can cause psychological distress in affected children and their parents. Recently, topical timolol has emerged as a new therapy option for treating uncomplicated IHs, but literature data are still lacking Objective: We aim to evaluate the efficacy and safety of topical timolol maleate 0,5% solution for treating superficial and mixed IHs Methods: A phase II, multicentre, randomized, double-blind, placebo-controlled, parallelgroup trial will be conducted during an estimated period of 2 years. Infants between 1 and 12 months with a focal, superficial or mixed IH will be recruited and randomly assigned to placebo and treatment groups. Efficacy will be assessed by performing blinded investigator photograph scoring and blinded volume measurements with ultrasound imaging at weeks 0, 1, 2, 3, 4, 8, 12, 16, 20 and 24. Safety will be assessed by measuring timolol in serum at week 4, and measuring heart rate and blood pressure and reporting adverse events at weeks 0, 1, 2, 3, 4, 8, 12, 20 and 24. Follow up will be carried out during 6 months in order to detect rebound

Country
Spain
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Keywords

Cancer in children -- Treatment, Càncer en els infants -- Tractament, Vasos sanguinis -- Càncer, Blood-vessels -- Cancer

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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Cancer Research