Example: Heart Attack
Clinical Trials on Hamartoma
Total 81 results
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NCT04485104Not yet recruitingConditions: Seizure in Participants With Tuberous Sclerosis Complex
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NCT04463316RecruitingConditions: Prader-Willi Syndrome; PWS-like Syndrome; Silver Russel Syndrome; Congenital Hypopituitarism; Klinefelter (XXY-)Syndrome; Congenital Adrenal Hyperplasia; XXXXY Syndrome; XXYY Syndrome; XXXX Syndrome (Tetra-X Syndrome); Disorders of Sex Development; Turner Syndrome; 46, XY DSD; Tuberous Sclerosis; Neurofibromatosis; Albright Hereditaire Osteodystrofie; Cornelia de Lange Syndrome; Saethre-Chotzen Syndrome; 17p- Deletiesyndrome; VCF Syndrome; POLR3A Mutatie; Ohdo Syndrome; Jacobsen Syndrome / 11 q Syndrome; Myrhe Syndrome; CHARGE Syndrome; 1q25-32 Deletie; Bardet Biedl Syndrome; Rett Syndrome; 22q11 Deletion Syndrome; Allan-Herndon-Dudley Syndrome; Kallmann Syndrome; Rare Bone Disorders; Noonan Syndrome; Williams-Beuren Syndrome
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NCT04344626RecruitingConditions: Epilepsy; Focal Cortical Dysplasia; Tuberous Sclerosis; Hemimegalencephaly; Polymicrogyria; Rasmussen Encephalitis; Sturge-Weber Syndrome; Gliosis; Stroke; Tumor, Brain
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NCT04316546RecruitingConditions: Proteus Syndrome
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NCT04285346RecruitingConditions: Tuberous Sclerosis
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NCT04198181Not yet recruitingConditions: Tuberous Sclerosis Complex; Epilepsy
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NCT04198207Not yet recruitingConditions: Tuberous Sclerosis Complex; Epilepsy
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NCT04112537Active, not recruitingConditions: Tuberous Sclerosis Complex
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NCT04094675RecruitingConditions: PTEN Gene Mutation; PTEN Hamartoma Tumor Syndrome; PTEN Hamartoma Syndrome; Cowden Syndrome; Bannayan Syndrome; Bannayan Zonana Syndrome; Polyposis
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NCT03826628RecruitingConditions: Facial Angiofibroma; Tuberous Sclerosis
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NCT03702309RecruitingConditions: Cancer; Breast Cancer; Lung Cancer; Colon Cancer; Ovarian Cancer; Melanoma; Lymphoma; Leukemia; Mutation; Lynch Syndrome; Cowden Syndrome; BRCA1 Mutation; BRCA2 Mutation; Uterine Cancer; Myeloma; Kidney Cancer; Head and Neck Cancer; Meningioma
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NCT03680924CompletedConditions: PTEN Gene Mutation
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NCT03630523Unknown statusConditions: PTEN Hamartoma Tumor Syndrome
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NCT03604055CompletedConditions: Airway Obstruction; Hamartoma of Lung
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NCT03525834Active, not recruitingConditions: Renal Angiomyolipoma
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NCT03422367RecruitingConditions: Tuberous Sclerosis
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NCT03382158RecruitingConditions: Pleuropulmonary Blastoma; Sertoli-Leydig Cell Tumor; DICER1 Syndrome; Cystic Nephroma; Wilms Tumor; Pineoblastoma; Renal Sarcoma; Nodular Hyperplasia of Thyroid; Nasal Chondromesenchymal Hamartoma; Ciliary Body Medulloepithelioma; Neuroblastoma; Pituitary Cancer; Embryonal Rhabdomyosarcoma
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NCT03363763RecruitingConditions: Angiofibroma of Face; Tuberous Sclerosis
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NCT03356769RecruitingConditions: Tuberous Sclerosis Complex; Aspirin; Epilepsy; Cognitive Decline; Skin Lesions
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NCT03326765RecruitingConditions: Sleep Disorder
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NCT03317366AvailableConditions: Proteus Syndrome; PIK3CA-Related Overgrowth Spectrum (PROS); Growth Disorders
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NCT03276195RecruitingConditions: Tuberous Sclerosis Complex
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NCT03254680WithdrawnConditions: Epilepsy; Dravet Syndrome; Lennox-Gastaut Syndrome; Tuberous Sclerosis; Focal Seizures
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NCT03140449CompletedConditions: Facial Angiofibroma
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NCT03094832RecruitingConditions: PIK3CA-Related Overgrowth Spectrum (PROS)/Proteus Syndrome
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NCT03050268RecruitingConditions: Acute Leukemia; Adenomatous Polyposis; Adrenocortical Carcinoma; AML; BAP1 Tumor Predisposition Syndrome; Carney Complex; Choroid Plexus Carcinoma; Constitutional Mismatch Repair Deficiency Syndrome; Diamond-Blackfan Anemia; DICER1 Syndrome; Dyskeratosis Congenita; Emberger Syndrome; Familial Acute Myeloid Leukemia; Familial Adenomatous Polyposis; Fanconi Anemia; Familial Cancer; Familial Wilms Tumor; Familial Neuroblastoma; GIST; Hereditary Breast and Ovarian Cancer; Hereditary Paraganglioma-Pheochromocytoma Syndrome; Hodgkin Lymphoma; Juvenile Polyposis; Li-Fraumeni Syndrome; Lynch Syndrome; MDS; Melanoma Syndrome; Multiple Endocrine Neoplasia Type 1; Multiple Endocrine Neoplasia Type 2; Neuroblastoma; Neurofibromatosis Type 1; Neurofibromatosis Type II; Nevoid Basal Cell Carcinoma Syndrome; Non Hodgkin Lymphoma; Noonan Syndrome and Other Rasopathy; Overgrowth Syndromes; Pancreatic Cancer; Peutz-Jeghers Syndrome; Pheochromocytoma/Paraganglioma; PTEN Hamartoma Tumor Syndrome; Retinoblastoma; Rhabdoid Tumor Predisposition Syndrome; Rhabdomyosarcoma; Rothmund-Thomson Syndrome; Tuberous Sclerosis; Von Hippel-Lindau Disease
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NCT02991807Active, not recruitingConditions: PTEN Gene Mutation; PTEN Hamartoma Tumor Syndrome
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NCT02962414Active, not recruitingConditions: Tuberous Sclerosis Complex
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NCT02887781RecruitingConditions: Tuberous Sclerosis Complex
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NCT02860494Not yet recruitingConditions: Facial Angiofibromas
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NCT02849457Active, not recruitingConditions: Tuberous Sclerosis Complex
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NCT02687633CompletedConditions: Tuberous Sclerosis Complex
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NCT02654340RecruitingConditions: Hypomelanotic Macules; Facial Angiofibroma; Shagreen Patches; Ungual Fibromas; Cortical Dysplasia; Cardiac Rhabdomyoma; Lymphangioleiomyomatosis; Renal Angiomyolipoma; Subependymal Giant Cell Astrocytoma
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NCT02635789CompletedConditions: Tuberous Sclerosis; Angiofibroma; Hypomelanotic Macule; Plaque
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NCT02634931CompletedConditions: Tuberous Sclerosis; Angiofibroma; Hypomelanotic Macule; Plaque
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NCT02594215Active, not recruitingConditions: Proteus Syndrome
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NCT02544750Enrolling by invitationConditions: Tuberous Sclerosis Complex; Seizures
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NCT02544763CompletedConditions: Tuberous Sclerosis Complex; Seizures
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NCT02461446RecruitingConditions: PTEN; ASD; Autism; Macrocephaly; PTEN Hamartoma Tumor Syndrome
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NCT02461459RecruitingConditions: Tuberous Sclerosis; Autism Disorder; Intellectual Disability
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NCT02451696CompletedConditions: Epilepsy; Tuberous Sclerosis Complex; Focal Cortical Dysplasia
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NCT02436746Unknown statusConditions: Neurofibromatosis Type I; Tuberous Sclerosis Complex
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NCT02325505RecruitingConditions: Tuberous Sclerosis; Lymphangioleiomyomatosis; Angiomyolipoma
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NCT02201212CompletedConditions: TSC1; TSC2; Tuberous Sclerosis Complex; MTOR
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NCT02104011CompletedConditions: Renal Angiomyolipomas; Tuberous Sclerosis
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NCT02098759Unknown statusConditions: TSC; Tuberous Sclerosis Complex; Epilepsy
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NCT02061397CompletedConditions: Lymphangioleiomyomatosis; Tuberous Sclerosis Complex
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NCT01954693Unknown statusConditions: Tuberous Sclerosis
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NCT01929642CompletedConditions: Tuberous Sclerosis Complex; Self-injury; Autism
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NCT01853423CompletedConditions: Facial Angiofibroma