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Peutz Jeghers syndrome

Peutz-Jeghers Syndrome
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-9 of 9 results.
Efficacy of Rapamycin (Sirolimus) in the Treatment of Peutz-Jeghers Syndrome
Status: Recruiting
Last Changed: Jan 23, 2019
First Received: Dec 19, 2018
Disease(s): Peutz-Jeghers Syndrome
Intervention(s): Rapamycin
Locations: Peking Union Medical College Hospital, Chinese Academy of Medicine Sciences, Beijing, China/Beijing, China
Study of Accurate Diagnosis and Treatment of Peutz-Jeghers Syndrome
Status: Recruiting
Last Changed: Jan 16, 2019
First Received: Jan 16, 2019
Disease(s): Peutz-Jeghers Syndrome
Intervention(s): Second generation sequencing, 16s rRNA gene sequencing
Locations: Changhai Hospital, Shanghai, China
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex
Status: Recruiting
Last Changed: Sep 12, 2019
First Received: Nov 04, 1999
Disease(s): Cushing's Syndrome, Pituitary Adenoma, Carney Complex, Primary Pigmented Nodular Adrenocortical Disease, Peutz-Jeghers Syndrome
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
The Cancer of the Pancreas Screening-5 CAPS5)Study
Status: Recruiting
Last Changed: Sep 16, 2019
First Received: Dec 03, 2013
Disease(s): Pancreas Cancer, Peutz-Jeghers Syndrome (PJS), Gene Mutation, Germline Mutation Carrier, Lynch Syndrome
Intervention(s): Human synthetic secretin
Locations: Yale University, New Haven, Connecticut, United States
Johns Hopkins Hospital, Baltimore, Maryland, United States
Dana Farber Cancer Center, Harvard University, Boston, Massachusetts, United States
University of Michigan, Ann Arbor, Michigan, United States
Columbia University Medical Center, New York, New York, United States
... and 4 other locations.
Pancreatic Cancer Early Detection Program
Status: Recruiting
Last Changed: Apr 30, 2019
First Received: Aug 01, 2014
Disease(s): 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
Intervention(s): Endoscopic Ultrasound, Magnetic Resonance Imaging (MRI)
Locations: White Plains Hospital, White Plains, New York, United States
Hereditary Gastric Cancer Syndromes: An Integrated Genomic and Clinicopathologic Study of the Predisposition to Gastric Cancer
Status: Recruiting
Last Changed: Sep 26, 2019
First Received: Jan 25, 2017
Disease(s): Stomach Neoplasms, Stomach Cancer, Familial Cancer, Fundic Gland Polyposis, Li-Fraumeni Syndrome, Lynch Syndrome, Peutz-Jeghers Syndrome
Locations: National Institutes of Health Clinical Center, Bethesda, Maryland, United States
Registry of Subjects at Risk of Pancreatic Cancer
Status: Recruiting
Last Changed: Sep 19, 2019
First Received: Sep 19, 2019
Disease(s): Familial Pancreatic Cancer, BRCA1 Mutation, BRCA2 Mutation, Lynch Syndrome, FAMMM - Familial Atypical Mole Malignant Melanoma Syndrome, Hereditary Pancreatitis, Peutz-Jeghers Syndrome
Intervention(s): MRCP, Endoultrasonography
Locations: Istituto Clinico Humanitas, Rozzano, Milan, Italy
Ospedale Pederzoli, Peschiera Del Garda, Verona, Italy
San Raffele Vita Salute University Hospital, Milano, Italy
Chirurgia Generale e del Pancreas, Verona, Italy
Familial Investigations of Childhood Cancer Predisposition
Status: Recruiting
Last Changed: Apr 26, 2019
First Received: Feb 10, 2017
Disease(s): 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
Locations: St. Jude Children's Research Hospital, Memphis, Tennessee, United States
Pancreas Registry and High Risk Registry
Status: Recruiting
Last Changed: Feb 27, 2019
First Received: May 17, 2016
Disease(s): Pancreas Cancer, Pancreatitis, Chronic Pancreatitis, Pancreatic Cyst, Family History of Pancreas Cancer, Genetic Mutations
Locations: Icahn School of Medicine at Mount Sinai, New York, New York, United States