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Klippel Trenaunay Syndrome clinical trials

View clinical trials related to Klippel Trenaunay Syndrome.

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NCT ID: NCT05563831 Recruiting - Clinical trials for Vascular Malformations

National Evaluation of Patients With PIK3CA-Related Overgrowth Spectrum (PROS)

COSY
Start date: February 21, 2023
Phase:
Study type: Observational

Overgrowth syndromes are rare genetic disorders defined by tissue hypertrophy that can be either localized or generalized, affecting both latitudinal and longitudinal growth. The genes involved in overgrowth syndromes are not well characterized but mostly concern the PIK3CA/AKT/mTOR pathway, a major actor of cell growth and proliferation. The mutations are not inherited but occurs during embryogenesis leading to somatic mosaicism. Owing to the variability of the clinical presentation, their exact prevalence is yet unknown. In order to answer this question, the investigators team create here the first French national registry on overgrowth syndromes.

NCT ID: NCT04836884 Completed - Clinical trials for Arteriovenous Malformations

Vascular Anomaly Pathology and Genomics Biopsy Study

Start date: April 6, 2021
Phase: N/A
Study type: Interventional

The purpose of this research is to gather information on the safety and effectiveness of core biopsy of vascular anomalies for clinical pathology and clinical genomics studies.

NCT ID: NCT03001180 Recruiting - Vascular Anomaly Clinical Trials

Identification of Biomarkers for Patients With Vascular Anomalies

Start date: April 2015
Phase:
Study type: Observational

The study will use blood (serum and plasma) and tissue obtained from participants undergoing prescribed surgical resection of vascular anomalies of interest proposed in this study. The study will also use blood (serum and plasma) and tissue collected and stored in a tissue bank maintained by the Department of Hematology/Oncology.

NCT ID: NCT02399527 Recruiting - Clinical trials for Lymphatic Malformation

Lymphatic Anomalies Registry for the Assessment of Outcome Data

Start date: June 2013
Phase:
Study type: Observational [Patient Registry]

Lymphatic anomalies are a rare subset of vascular anomalies that are poorly understood. the understanding of the natural history, long-term outcomes, risk factors for morbidity and mortality, and the relative benefit of medical therapies and procedures is limited.The goal of this project is to better understand these diseases and improve the care of theses rare patients. To do this, the investigators are conducting an observational study of patients with lymphatic anomalies, including an annual follow-up questionnaire to gather prospective data on mortality, morbidity, treatments, and functionality as well as quality of life.

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.