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Hemangioma, Capillary clinical trials

View clinical trials related to Hemangioma, Capillary.

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NCT ID: NCT01512173 Completed - Clinical trials for Infantile Hemangioma

Study in Infants With Infantile Hemangioma to Compare Propranolol Gel to Placebo

Start date: January 2012
Phase: Phase 2
Study type: Interventional

There is an unsatisfied medical need for a first-line treatment of localized uncomplicated proliferating Infantile Hemangioma with a good benefit/risk profile. Pierre Fabre Dermatologie has developed a new formulation of propranolol (V0400 GL 01A) which is a topical gel adapted to paediatric use. The objective of this study is to evaluate topical propranolol efficacy and safety in the management of localized hemangioma.

NCT ID: NCT01438047 Withdrawn - Port Wine Stain Clinical Trials

Optical Frequency Domain Imaging (OFDI) in Dermatology

Start date: September 2010
Phase: N/A
Study type: Observational

This is a pilot exploratory study. The goal of this study is to evaluate a new imaging tool, optical frequency domain imaging (OFDI), to reveal the microvascular morphology of capillary malformations.

NCT ID: NCT01434849 Terminated - Clinical trials for Very Low Birth Weight Infants

Timolol for the Prevention of Proliferation of Infantile Hemangioma (TiPPIH Trial)

TiPPIH
Start date: July 2012
Phase: Phase 1
Study type: Interventional

The purpose of this trial is to see if a topical beta blocker is effective in preventing the proliferation of infantile hemangioma.

NCT ID: NCT01431326 Completed - Hypertension Clinical Trials

Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care

PTN_POPS
Start date: November 2011
Phase:
Study type: Observational

Understudied drugs will be administered to children per standard of care as prescribed by their treating caregiver and only biological sample collection during the time of drug administration will be involved. A total of approximately 7000 children aged <21 years who are receiving these drugs for standard of care will be enrolled and will be followed for up a maximum of 90 days. The goal of this study is to characterize the pharmacokinetics of understudied drugs for which specific dosing recommendations and safety data are lacking. The prescribing of drugs to children will not be part of this protocol. Taking advantage of procedures done as part of routine medical care (i.e. blood draws) this study will serve as a tool to better understand drug exposure in children receiving these drugs per standard of care. The data collected through this initiative will also provide valuable pharmacokinetic and dosing information of drugs in different pediatric age groups as well as special pediatric populations (i.e. obese).

NCT ID: NCT01408056 Withdrawn - Clinical trials for Infantile Hemangiomas

Timolol Option for Ulcerated Hemangiomas (TOUCH Trial)

TOUCH
Start date: February 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Timolol 0.5% Gel Forming Solution is safe and effective in promoting wound healing of infantile ulcerated hemangiomas compared with standard conservative management with topical antibiotic.

NCT ID: NCT01364857 Completed - Port Wine Stain Clinical Trials

French National Cohort of Children With Port Wine Stain

CONAPE
Start date: November 2010
Phase: N/A
Study type: Interventional

Port Wine Stain on a limb can be either isolated or associated with complications (venous or orthopedic impairment, arteriovenous malformations), leading sometimes to complex syndromes (Klippel-Trenaunay syndrome,Parkes-Weber syndrome). Little is known about epidemiology of port wine stains: their evolution during the growth of the child, the frequency of complications, genetic data, and prognostic factors. This prospective french national cohort will help for : description of the evolution of port wine stain and possible complications; prognostic factors for complications ; association with mutations of RASA1 gene; quality of life of these children. It will also help for global appreciation of the management of this disease in France.

NCT ID: NCT01333553 Completed - PORT WINE STAIN Clinical Trials

Monitoring the Response of Port Wine Stain Birthmarks to Laser Therapy With Wide-field Functional Imaging Technologies

Start date: April 2010
Phase:
Study type: Observational

The researcher develop non-invasive imaging modalities for assessment of port wine stain during laser therapy treatment of Port Wine Stain. The imaging modalities will be used to guide immediate retreatment of regions of persistent perfusion during the procedure.

NCT ID: NCT01272609 Recruiting - Melanoma Clinical Trials

Treatment of Port Wine Stains in Children With Pulsed Dye Laser and Timolol Gel

Start date: January 2011
Phase: Phase 3
Study type: Interventional

Pulsed dye laser (PDL)is the gold standard treatment of port wine stains (PWS). However, many sessions are required and failure or relapses are not uncommon. It has been demonstrated that a neoangiogenesis occurs after PDL, explaining at least partially those failure. The objective of this study is to evaluate the use of a topical beta-blocker (timolol 1% gel) as a combination treatment with PDL for treating PWS. Methods. Prospective multicenter study comparing PDL alone to PDL + timolol. Sessions of PDL will be performed once a month for 3 months. One group will be treated with PDL alone and the other will also applied timolol 1% gel twice a day during treatment. The evaluation will be done one month after the third session.

NCT ID: NCT01166919 Withdrawn - Port Wine Stain Clinical Trials

Pilot Study on the Use of the Matrix Radiofrequencyfor Treatment of Port Wine Stain Birthmarks

Start date: December 2009
Phase: Phase 1
Study type: Interventional

Port wine stain, also called nevus flammeus, is a congenital, cutaneous vascular malformation involving post-capillary venules which produces a light pink to red to dark-red-violet discoloration of the skin. It is estimated that Port wine stain occurs in 3 children per 1,000 live births. Approximately 900,000 individuals in the United States and twenty million people worldwide have Port wine stain birthmarks .

NCT ID: NCT01147601 Recruiting - Infant Clinical Trials

Topical Timolol 0.5% Solution for Proliferating Infantile Hemangiomas

Start date: March 2010
Phase: Phase 0
Study type: Interventional

The purpose of this study is to learn about a new potential use for topical timolol 0.5% aqueous solution that may help treat small uncomplicated infantile hemangiomas. This study would examine whether topical timolol could be a potential therapy.