Klinische Studien zur Peutz-Jeghers-Syndrom

Insgesamt 16 ergebnisse





    • NCT03781050
      Rekrutierung
      Bedingungen: Peutz-Jeghers Syndrome
    • NCT03806075
      Rekrutierung
      Bedingungen: Peutz-Jeghers Syndrome
    • NCT00811590
      Beendet
      Bedingungen: Peutz-Jeghers Syndrome
    • NCT01178151
      Zurückgezogen
      Bedingungen: Peutz-Jeghers Syndrome; Neoplastic Processes; Neoplasm Metastasis
    • NCT00438906
      Abgeschlossen
      Bedingungen: Pancreatic Neoplasm; Peutz-Jeghers Syndrome
    • NCT00001452
      Abgeschlossen
      Bedingungen: Cushing's Syndrome; Pituitary Adenoma; Carney Complex; Primary Pigmented Nodular Adrenocortical Disease; Peutz-Jeghers Syndrome
    • NCT00633607
      Abgeschlossen
      Bedingungen: Lynch Syndrome; FAP; Hereditary Diffuse Gastric Cancer; Juvenile Polyposis Syndrome; Peutz-Jeghers Syndrome
    • NCT02000089
      Rekrutierung
      Bedingungen: Pancreas Cancer; Peutz-Jeghers Syndrome (PJS); Gene Mutation; Germline Mutation Carrier; Lynch Syndrome
    • NCT02206360
      Rekrutierung
      Bedingungen: Pancreatic Cancer; Pancreas Cancer; Pancreatic Adenocarcinoma; Familial Pancreatic Cancer; BRCA 1/2; HNPCC; Lynch Syndrome; Hereditary Pancreatitis; FAMMM; Familial Atypical Multiple Mole Melanoma; Peutz Jeghers Syndrome
    • NCT04095195
      Rekrutierung
      Bedingungen: Familial Pancreatic Cancer; BRCA1 Mutation; BRCA2 Mutation; Lynch Syndrome; FAMMM - Familial Atypical Mole Malignant Melanoma Syndrome; Hereditary Pancreatitis; Peutz-Jeghers Syndrome
    • NCT03050268
      Rekrutierung
      Bedingungen: 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
    • NCT01656746
      Abgeschlossen
      Bedingungen: Adenomatous Polyp; Crohn Disease; Familial Adenomatous Polyposis; Hereditary Intestinal Polyposis Syndrome; Recurrent Colon Cancer; Stage I Colon Cancer; Stage IIA Colon Cancer; Stage IIB Colon Cancer; Stage IIC Colon Cancer; Stage IIIA Colon Cancer; Stage IIIB Colon Cancer; Stage IIIC Colon Cancer
    • NCT00587132
      Beendet
      Bedingungen: Pancreatic Cancer
    • NCT02309632
      Zurückgezogen
      Bedingungen: Pancreatic Neoplasms; Peutz-Jegher's Syndrome; BRCA1 Gene Mutation; BRCA2 Gene Mutation; Ataxia Telangiectasia; Familial Atypical Mole-Malignant Melanoma Syndrome; Colorectal Neoplasms, Hereditary Nonpolyposis; Hereditary Pancreatitis
    • NCT02775461
      Rekrutierung
      Bedingungen: Pancreas Cancer; Pancreatitis; Chronic Pancreatitis; Pancreatic Cyst; Family History of Pancreas Cancer; Genetic Mutations
    • NCT00040222
      Abgeschlossen
      Bedingungen: Familial Ovarian Cancer; Familial Breast Cancer; BRCA1-associate Malignancies; BRCA2-associated Malignancies