Red de Apoyo a la Investigación, Coordinación de la Investigación Científica, Universidad Nacional Autónoma de México | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients	Abnormalities, Multiple, Adenoma, Islet Cell, Carcinoma, Medullary, Carney complex, Carney triad, Carney-Stratakis syndrome, Ciliopathies, Colorectal Neoplasms, Hereditary Nonpolyposis, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cowden disease, DICER1-related tumor predisposition, DNA repair disease, Digestive System Diseases, Digestive System Neoplasms, Li-Fraumeni syndrome, Lynch syndrome, Malformations of Cortical Development, Group I, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Connective and Soft Tissue, Neoplasms, Ductal, Lobular, and Medullary, Neoplasms, Germ Cell and Embryonal, Neoplasms, Multiple Primary, Neoplasms, Nerve Tissue, Nutritional and Metabolic Diseases, Pituitary Adenoma, Familial Isolated, Pituitary Neoplasms, Skin Abnormalities, Thoracic Neoplasms, adenocarcinoma, adenoma, angiomatosis, brain disorder, carcinoma, cardiovascular disorder, central nervous system cancer, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, colonic disorder, colorectal neoplasm, connective tissue neoplasm, digestive system disorder, digestive system neoplasm, endocrine system disorder, epithelial neoplasm, familial isolated pituitary adenoma, gastrointestinal stromal tumor, hamartoma, heart cancer, heart disorder, hereditary disease, hereditary neoplastic syndrome, hyperparathyroidism, hypothalamic disorder, hypothalamic neoplasm, inherited neurodegenerative disorder, intestinal disorder, lung neuroendocrine neoplasm, malignant endocrine neoplasm, medullary thyroid gland carcinoma, metabolic disease, multiple endocrine neoplasia, multiple endocrine neoplasia type 1, multiple endocrine neoplasia type 2A, multiple endocrine neoplasia type 4, myxoma, neoplasm, nerve sheath neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, neuroendocrine carcinoma, neuroendocrine neoplasm, neurofibroma, neurofibromatosis, neurofibromatosis type 1, neuromuscular disease, pancreas disorder, pancreatic neoplasm, paraganglioma, parathyroid gland disorder, peripheral nervous system disorder, pheochromocytoma, pituitary gland disorder, primary hyperparathyroidism, primitive neuroectodermal tumor, supratentorial cancer, tuberous sclerosis, vascular disorder, von Hippel-Lindau disease	Recruiting	Not stated	2024-07-26		NCT06523582