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Bardet-Biedl Syndrome

Laurence-Moon-Bardet-Biedl syndromeLaurence-Moon syndrome
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-10 of 10 results.
Clinical Registry Investigating Bardet-Biedl Syndrome
Status: Recruiting
Last Changed: Aug 11, 2020
First Received: Dec 31, 2014
Disease(s): Bardet-Biedl Syndrome
Locations: Marshfield Clinic Research Foundation, Marshfield, Wisconsin, United States
Genetics and Clinical Characteristics of Bardet-Biedl Syndrome
Status: Terminated
Last Changed: Dec 04, 2019
First Received: Feb 19, 2004
Disease(s): Bardet-Biedl Syndrome
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
Bardet-Biedl Syndrome Study: Clinical and Genetic Epidemiology Study in Adults
Status: Completed
Last Changed: Aug 08, 2008
First Received: Sep 21, 2005
Disease(s): Bardet-Biedl Syndrome, Orphan Diseases
Intervention(s): clinical, biological, and radiological
Locations: Hélène Dollfus, Strasbourg, France
Treatment of Bardet-Biedl-Syndrome With Metformin for Evaluation of a Possible Visual Improvement
Status: Withdrawn
Last Changed: Apr 18, 2019
First Received: Apr 06, 2018
Disease(s): Bardet-Biedl Syndrome, Visual Impairment
Intervention(s): Metformin
Setmelanotide (RM-493), Melanocortin-4 Receptor (MC4R) Agonist, in Bardet-Biedl Syndrome (BBS) and Alström Syndrome (AS) Patients With Moderate to Severe Obesity
Status: Active, not recruiting
Last Changed: Jun 22, 2020
First Received: Nov 19, 2018
Disease(s): Bardet Biedl Syndrome (BBS), Alström Syndrome (AS)
Intervention(s): Setmelanotide, Placebos
Locations: Wr-McCr, Llc, San Diego, California, United States
UMMS Baystate Health; BAYSTATE MEDICAL CENTER; Baystate Children's Specialty Center, Springfield, Massachusetts, United States
Columbia University Center, New York, New York, United States
M3 Wake Research, Raleigh, North Carolina, United States
University of Tennessee Health Science Center, Memphis, Tennessee, United States
... and 9 other locations.
COhort for Bardet-Bield Syndrome and Alström Syndrome for Translational Research Monocentric Interventional Study
Status: Recruiting
Last Changed: Jul 08, 2020
First Received: Jul 08, 2020
Disease(s): Bardet-Biedl Syndrome, Alström Syndrome
Intervention(s): Skin biopsy
Locations: Les Hôpitaux Universitaires de Strasbourg, Strasbourg, France
Setmelanotide Phase 2 Treatment Trial in Patients With Rare Genetic Disorders of Obesity
Status: Recruiting
Last Changed: Jul 29, 2020
First Received: Jan 06, 2017
Disease(s): Pro-opiomelanocortin (POMC) Deficiency Obesity (Heterozygous or Epigenetic), Leptin Receptor Deficiency Obesity, Bardet-Biedl Syndrome, Alstrom Syndrome, Smith-Magenis Syndrome
Intervention(s): Setmelanotide
Locations: Synexus Clinical Research US, Inc. - Simon Williamson Clinic, PC, Birmingham, Alabama, United States
Synexus Clinical Research US, Inc. - Phoenix Southeast, Chandler, Arizona, United States
Synexus Clinical Research US, Inc. - Central Arizona Medical Associates, PC, Mesa, Arizona, United States
Honor Health Research Institute, Scottsdale, Arizona, United States
Axis Clinical Trials-Downtown, Los Angeles, California, United States
... and 45 other locations.
GROWing Up With Rare GENEtic Syndromes
Status: Recruiting
Last Changed: Jul 09, 2020
First Received: Jul 09, 2020
Disease(s): 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
Intervention(s): Retrospective file studies
Locations: Erasmus Medical Center, Rotterdam, Zuid-Holland, Netherlands
Inherited Retinal Degenerative Disease Registry
Status: Recruiting
Last Changed: Dec 13, 2018
First Received: May 06, 2015
Disease(s): Eye Diseases Hereditary, Retinal Disease, Achromatopsia, Bardet-Biedl Syndrome, Bassen-Kornzweig Syndrome, Batten Disease, Best Disease, Choroidal Dystrophy, Choroideremia, Cone Dystrophy, Cone-Rod Dystrophy, Congenital Stationary Night Blindness, Enhanced S-Cone Syndrome, Fundus Albipunctatus, Goldmann-Favre Syndrome, Gyrate Atrophy, Juvenile Macular Degeneration, Kearns-Sayre Syndrome, Leber Congenital Amaurosis, Refsum Syndrome, Retinitis Pigmentosa, Retinitis Punctata Albescens, Retinoschisis, Rod-Cone Dystrophy, Rod Dystrophy, Rod Monochromacy, Stargardt Disease, Usher Syndrome
Locations: Foundation Fighting Blindness, Columbia, Maryland, United States
UAB HRFD Core Center: Core A: The Hepato/Renal Fibrocystic Diseases Translational Resource
Status: Recruiting
Last Changed: Oct 25, 2019
First Received: Jul 26, 2011
Disease(s): Hepato/Renal Fibrocystic Disease, Autosomal Recessive Polycystic Kidney Disease, Joubert Syndrome, Bardet Biedl Syndrome, Meckel-Gruber Syndrome, Congenital Hepatic Fibrosis, Caroli Syndrome, Oro-Facial-Digital Syndrome Type I, Nephronophthisis, Glomerulocystic Kidney Disease
Locations: Children's National Health System, Washington, District of Columbia, United States