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Trial Match

Clinical trials test new treatments โ€” sometimes the newest options available for a disease. Find trials that are recruiting now, near you. Open one to see its eligibility rules as simple questions to go through with your doctor.

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30 recruiting trials

for Lymphatic Malformations

Weekly Sirolimus Therapy NCT04861064Phase 21 site๐Ÿ“ Charleston Medical University of South Carolina ยท Tests: Sirolimus Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford NCT01793168n/a1 site๐Ÿ“ Sioux Falls Sanford Health Understanding of Psychotic Disorders in Children With 22q11.2DS NCT04639388NA1 site๐Ÿ“ Lyon Hรดpital le Vinatier ยท Tests: neuropsychological testing, questionnaires and experimental tasks Study of the Disease Process of Lymphangioleiomyomatosis NCT00001465n/a1 site๐Ÿ“ Bethesda National Heart, Lung, and Blood Institute (NHLBI) ยท Tests: Toshibia Aquilion One CT Quality of Life in Pediatric Participants With HHT NCT07474428n/a1 site๐Ÿ“ Cincinnati Ashley Nelson Efficacy of Rapamycin in the Treatment of Cervico-facial Lymphatic Malformations NCT03243019Phase 22 sites๐Ÿ“ Lille๐Ÿ“ Paris University Hospital, Lille ยท Tests: rapamycin, MRI, Rapamycin dosage Lymphatic Anomalies Registry for the Assessment of Outcome Data NCT02399527n/a1 site๐Ÿ“ Boston Boston Children's Hospital A Prospective Natural History Study of Lymphatic Anomalies NCT05731141n/a2 sites๐Ÿ“ Bethesda๐Ÿ“ Philadelphia Eunice Kennedy Shriver National Institute of Child Health aโ€ฆ Body Donation in HHT NCT07826845NA1 site๐Ÿ“ Essen University Hospital, Essen ยท Tests: body donation in HHT Institution of an Italian Registry and Biobank for Biological Sample Collection NCT06892964NA1 site๐Ÿ“ Roma Fondazione Policlinico Universitario Agostino Gemelli IRCCS ยท Tests: Genetic profiling of all eligible patients GROWing Up With Rare GENEtic Syndromes NCT04463316n/a1 site๐Ÿ“ Rotterdam dr. Laura C. G. de Graaff-Herder ยท Tests: Retrospective file studies The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome NCT00768820Phase 41 site๐Ÿ“ Petah Tikva The Chaim Sheba Medical Center ยท Tests: methylphenidate, fluoxetin, risperidone Non-Invasive Detection of Pulmonary Right-to-Left Shunts Using the SONAS Ultrasound Device NCT07414446NA1 site๐Ÿ“ Nieuwegein St. Antonius Hospital ยท Tests: Transcranial Ultrasound Device Hematopoietic Stem Cell Transplantation (HSCT) for Common Variable Immunodeficiency (CVID) and Other Autoimmune Manifestations of Primary Immune Regulatory Disorders (PIRD) NCT07284641Phase 21 site๐Ÿ“ Pittsburgh Paul Szabolcs ยท Tests: Hematopoietic stem cell transplant (HSCT) Identification of Biomarkers for Patients with Vascular Anomalies NCT03001180n/a2 sites๐Ÿ“ Boston๐Ÿ“ Cincinnati Children's Hospital Medical Center, Cincinnati Familial Investigations of Childhood Cancer Predisposition NCT03050268n/a1 site๐Ÿ“ Memphis St. Jude Children's Research Hospital HPB-092 for the Treatment of Relapsed and Refractory Acute Myeloid Leukemia NCT07137637Phase 11 site๐Ÿ“ Tianjin Hangzhou Polymed Biopharmaceuticals, Inc. ยท Tests: HPB-092 tablet A Trial to Assess the Efficacy and Safety of Engasertib in Participants With Moderate to Severe Hereditary Hemorrhagic Telangiectasia (HHT) NCT07743671Phase 34 sites๐Ÿ“ Chicago๐Ÿ“ Indianapolis๐Ÿ“ Rochester Vaderis Therapeutics AG ยท Tests: Engasertib, Placebo Vascular Lab Resource (VLR) Biorepository NCT05628948n/a1 site๐Ÿ“ Cleveland The Cleveland Clinic Molecular Studies on Hereditary Haemorrhagic Telangiectasia Families NCT00230620n/a1 site๐Ÿ“ London Imperial College London Case Notes Review on Patients With Hereditary Haemorrhagic Telangiectasia NCT00230685n/a1 site๐Ÿ“ London Imperial College London Prospective Study of Antiplatelet and Anticoagulation Therapy in Hereditary Haemorrhagic Telangiectasia NCT05641142NA18 sites๐Ÿ“ Angers๐Ÿ“ Bordeaux๐Ÿ“ Boulogne-Billancourt University Hospital, Clermont-Ferrand ยท Tests: monitoring the use of anticoagulant and/or antiplatelet therapy in patients with osler rendering disease Intensive Multimodal Neurorehabilitation Targeting Neuroplasticity in Pediatric Neurodevelopmental and Chromosomal Disorders NCT07493096n/a1 site๐Ÿ“ The Woodlands Healing Hope International TSC Biosample Repository and Natural History Database NCT05676099n/a26 sites๐Ÿ“ Birmingham๐Ÿ“ Loma Linda๐Ÿ“ Los Angeles National Tuberous Sclerosis Association ยท Tests: Phlebotomy, Buccal (cheek) swab, Genetic Testing, Tissue donation after routine clinical procedure The ADVANCE (Assay Development and Validation for Pre-Natal and Obstetric Conditions) Study is the Largest U.S.-Based Prospective Study Demonstrating a Circulating Fetal Cell (CFC) Based Approach to Non-invasive Fetal Risk Assessment NCT07643896n/a9 sites๐Ÿ“ Phoenix๐Ÿ“ Riverside๐Ÿ“ West Covina BillionToOne Inc. Efficacy of Nintedanib for Treatment of Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT) Patients NCT04976036Phase 23 sites๐Ÿ“ Bron๐Ÿ“ Clermont-Ferrand๐Ÿ“ Lausanne Dr. Romain Lazor ยท Tests: Nintedanib, Placebo European Registry Study on Lymphatic Interventions NCT07131293n/a1 site๐Ÿ“ Copenhagen Copenhagen University Hospital, Rigshospitalet ยท Tests: Lymphatic intervention A Study to Investigate Efficacy and Safety of KP-001 Compared With Placebo in Patients Aged โ‰ฅ2 Years With Common VM, Common LM, or KTS/CLOVES Syndrome NCT07285005Phase 35 sites๐Ÿ“ Charleston๐Ÿ“ Daegu๐Ÿ“ Seoul Kaken Pharmaceutical ยท Tests: KP-001, Placebo Alpelisib in Pediatric and Adult Patients With Lymphatic Malformations Associated With a PIK3CA Mutation. NCT05948943Phase 2, Phase 361 sites๐Ÿ“ Oakland๐Ÿ“ Orange๐Ÿ“ Palo Alto Novartis Pharmaceuticals ยท Tests: Alpelisib, Placebo Influence of Hypoxic Induced Factors in Patients With Hereditary Hemorrhagic Telangiectasia NCT04469517n/a1 site๐Ÿ“ Essen University Hospital, Essen ยท Tests: hypoxic induced factors
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