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Hemangioma clinical trials

View clinical trials related to Hemangioma.

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NCT ID: NCT02079818 Withdrawn - Clinical trials for Arteriovenous Malformations

Visceral Artery Aneurysm Embolization by the Penumbra Ruby™ Coil System

Start date: June 2017
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to gather post market data on the Penumbra Ruby Coil System in the treatment of visceral artery aneurysms and arteriovenous malformations. This study is a prospective, multi-center study of patients with visceral artery aneurysms and visceral arteriovenous malformations who are treated by the Penumbra Ruby Coil System. Data for each patient are collected up to 12 months post-procedure for the study.

NCT ID: NCT01408056 Withdrawn - Clinical trials for Infantile Hemangiomas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NCT ID: NCT00974129 Withdrawn - Hemangioma Clinical Trials

A Study of CCCTC-binding Factor (CTCF) in Infantile Hemangiomas

Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the genotype of CTCF, a proven transcription factor, in patients with infantile hemangiomas and to monitor tumor growth. The investigators aim to determine whether or not the CTCF genotype might serve as an early and reliable predictor of tumor growth.

NCT ID: NCT00733759 Withdrawn - Clinical trials for Pulmonary Arteriovenous Malformations

Contrast Echocardiography in Patients With Pulmonary Arteriovenous Malformations (PAVMs)

Start date: February 2004
Phase:
Study type: Observational

Pulmonary arteriovenous malformations (PAVMs) are thin-walled abnormal vessels which provide direct capillary-free communications between the pulmonary and systemic circulations. Patients with PAVMs have usually have low blood oxygen levels and are at risk of other complications including strokes, brain abscesses, pregnancy-related complications and haemorrhage. We hypothesise that the complications of PAVM patients arise from their PAVMs and not the more recognised intracardiac forms of shunting. We propose to perform echocardiograms to enable assessment of the presence of other causes of capillary-free communications between the pulmonary and systemic circulations.