Search clinical trials for: Syndromic

Total 43 results

Beny Lafer

Recruiting

ACT for Syndromic and Subsyndromic Depression in Bipolar Disorder

Bipolar Disorder

Brazil
University Hospital, Bordeaux

Not yet recruiting

Genetic Research of Monogenic Obesity in a Pediatric Cohort With Severe and Early Onset Obesity (GENOBE) (GENOBE)

Monogenic Obesity | Non Syndromic Obesity

France
Riccardo Serraino
Societa' Italiana Di Malattie Infettive E Tropicali

Recruiting

Utility and Acceptability of a Molecular Test in the Management of Sexually Transmitted Diseases in Uganda (ASTRHA)

Sexually Transmitted Diseases

Uganda
Centre Hospitalier Universitaire Dijon

Recruiting

Study of the Value of Trio Exome Sequencing in the Etiological Assessment of Specific Non-syndromic Language and Learning Disorders (TSLA ES)

Specific Language and Learning Disorders (SLLD)

France
Hospices Civils de Lyon

Not yet recruiting

SEMASEARCH, Retrospective/Prospective Cohort Nested at ATUc/AP2 WEGOVY® (SEMASEARCH)

Obesity | Sarcopenic Obesity | Bariatric Surgery | Binge Eating Disorder | Psychotropic Drugs | Syndromic Obesity | Iatrogenic Obesity

France
University Hospital, Montpellier

Not yet recruiting

Multidisciplinary Evaluation and a Genome-wide Analysis in a Cohort of Idiopathic Short Stature Patients (PAG PETI)

Idiopathic Short Stature
Chinese Medical Association

Recruiting

Study on Susceptibility Genes and Pathogenic Mechanism of Non-syndromic Familial Aortic Dissection

Aortic Dissection | Family Research | Aortic Dissection, Familial, With or Without Aortic Aneurysm

China
Assistance Publique - Hôpitaux de Paris

Recruiting

Trial on a Strategy Combining Rapid Diagnostic Testing and Antimicrobial Stewardship to Improve Antibiotic Use in Patients With Hospital-acquired Pneumonia. (SHARP)

Hospital-acquired Pneumonia

France
GenSight Biologics

Recruiting

Dose-escalation Study to Evaluate the Safety and Tolerability of GS030 in Subjects With Retinitis Pigmentosa (PIONEER)

Non-syndromic Retinitis Pigmentosa

United States, France, United Kingdom
Hôpital le Vinatier
Hospices Civils de Lyon

Recruiting

Validation of a Clinical Screening Grid for Syndromic Schizophrenia (Schizo-CGH-EXM)

Schizophrenia

France
Sanford Health
National Ataxia Foundation; Beyond Batten Disease Foundation; Pitt Hopkins Research... and other collaborators

Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford (CoRDS)

Mitochondrial Diseases | Retinitis Pigmentosa | Myasthenia Gravis | Eosinophilic Gastroenteritis | Multiple System Atrophy | Leiomyosarcoma | Leukodystrophy | Anal Fistula | Spinocerebellar Ataxia Type 3 | Friedreich Ataxia | Kennedy Disease | Lyme Disease | Hemophagocytic Lymphohistiocytosis | Spinocerebellar Ataxia... and other conditions

United States, Australia
Simons Searchlight
Boston Children's Hospital; Geisinger Clinic; Simons Foundation

Recruiting

Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

SMARCA4 Gene Mutation | DDX3X | 16P11.2 Deletion Syndrome | 16p11.2 Duplications | 1Q21.1 Deletion | 1Q21.1 Microduplication Syndrome (Disorder) | ACTL6B | ADNP | AHDC1 | ANK2 | ANKRD11 | ARID1B | ASH1L | BCL11A | CHAMP1 | CHD2 | CHD8 | CSNK2A1 | CTBP1 | CTNNB1 Gene Mutation | CUL3 | DNMT3A | DSCAM | DYRK1A | FOXP1 | GRIN2A | GRIN2B | HIVEP2-Related Intellectual... and other conditions

United States
National Institute on Deafness and Other Communication...

Enrolling by invitation

Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan

Hearing Disorder

Pakistan
Rush University Medical Center
Emory University

Enrolling by invitation

Promoting Prosocial Behavior in Syndromic Intellectual and Developmental Disabilities

Tuberous Sclerosis | Fragile X Syndrome | Rett Syndrome | Hamartoma Syndrome, Multiple | Angelman Syndrome | Creatine Deficiency, X-linked | Telomeric 22Q13 Monosomy Syndrome | Chromosome 15Q, Partial Deletion

United States
Eunice Kennedy Shriver National Institute of Child...
National Institutes of Health (NIH)

Terminated

Genetic Causes of Growth Disorders

Short Stature | Growth Disorder | Syndromic Growth Disorder | Tall Stature

United States
Johns Hopkins Bloomberg School of Public Health
Pontificia Universidad Javeriana

Completed

Digital Applications to Monitor Novel Coronavirus Disease and Response in Colombia - Syndromic and Vaccination Surveillance (DIAMOND-R)

COVID-19 | Vaccination Refusal

United States
ProQR Therapeutics

Terminated

Study to Evaluate the Efficacy Safety and Tolerability of QR-421a in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene With Early to Moderate Vision Loss (Celeste)

Eye Diseases | Retinitis Pigmentosa | Eye Diseases, Hereditary | Vision Disorders | Retinal Disease | Eye Disorders Congenital | Usher Syndrome Type 2 | Deaf Blind

United States, United Kingdom
ProQR Therapeutics

Active, not recruiting

Study to Evaluate the Efficacy Safety and Tolerability of Ultevursen in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene (Sirius)

Eye Diseases | Retinitis Pigmentosa | Eye Diseases, Hereditary | Vision Disorders | Retinal Disease | Eye Disorders Congenital | Usher Syndrome Type 2 | Deaf Blind

United States, Netherlands, United Kingdom, Germany
Assistance Publique - Hôpitaux de Paris
Institut National de la Santé Et de la Recherche Médicale, France

Completed

Phenotypic and Genotypic Characterization of Subjects With Syndromic Obesity: Identifying New Candidate Genes by Exome Sequencing (OBEXOME) (OBEXOME)

Syndromic Obesity

France
Assistance Publique - Hôpitaux de Paris
French rare diseases Healthcare Network; The French Foundation for Rare Diseases

Active, not recruiting

Non-syndromic Inherited Anomalies of Mineralized Tooth Tissues: a Whole Exome Study to Identify New Pathogenic Variants (EXODENT)

Amelogenesis Imperfecta | Dentinogenesis Imperfecta | Dentin Anomalies

France
University of Leicester

Active, not recruiting

A Study to Evaluate the Feasibility of Screening Relatives of Patients Affected by Non-Syndromic Thoracic Aortic Diseases (ReST)

Genetic Disease | Screening | Aortic Aneurysm and Dissection

United Kingdom
Centre Hospitalier Universitaire de Besancon

Completed

Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study (SHD-DI)

Severe Intellectual Disability

France
University Hospital, Montpellier
Association Xtraordinaire sub-group DDX3X; Genida

Unknown

Better Delineation of DDX3X Related Phenotype and Epigenetic Signature.

Intellectual Developmental Disorder | X-LINKED

France
National Human Genome Research Institute (NHGRI)

Completed

Genetic Analysis of Hereditary Non-Syndromic Oral Clefts

Hereditary Oral Clefts

Syrian Arab Republic
Growing Spine Study Group
Growing Spine Foundation

Completed

The Treatment of Progressive Early Onset Spinal Deformities: A Multi-Center Outcome Study (GSSG)

Early Onset Scoliosis | Thoracic Insufficiency Syndrome | Congenital Spinal Deformities | Infantile Idiopathic Scoliosis | Neuromuscular Spinal Deformity | Syndromic Spinal Deformity

United States, Canada, United Kingdom, Egypt, Ghana, Spain, Turkey
National Institute on Deafness and Other Communication...

Terminated

Genetic Analysis of Human Hereditary Hearing Impairment

Partial Hearing Loss

United States
National Eye Institute (NEI)

Completed

Natural History and Genetic Studies of Usher Syndrome

Retinitis Pigmentosa | Usher Syndrome | Retinitis Pigmentosa Syndromic | Congenital Deafness | Retinitis Pigmentosa and Deafness

United States
Janneke van de Wijgert
Institute of Tropical Medicine, Belgium; Rinda Ubuzima, Rwanda

Completed

Women's Improvement of Sexual Health (WISH) Demonstration Project (WISH)

Urinary Tract Infections | Vaginal Candidiasis | Bacterial Vaginosis | Sexually Transmitted Disease

Rwanda
Imperial College London
Biomedical Research and Training Institute

Completed

Scientific Evaluation of Peer Education and STD Treatment to Reduce the Spread of HIV in Zimbabwe

HIV Infections

Zimbabwe
Avera McKennan Hospital & University Health Center

Withdrawn

Continuous Temperature Measurement for Syndromic Surveillance

Continuous Temperature | Syndromic Surveillance | Long-term Care

United States
Rennes University Hospital

Completed

Non Syndromic Congenital Heart Defect and Array-CGH in Prenatal Diagnosis (CAPA)

Non Syndromic Congenital Heart

France
Novartis Pharmaceuticals

Completed

RAMSETE: RAD001 in Advanced and Metastatic Silent Neuro-endocrine Tumors in Europe (RAMSETE/CDE16)

Carcinoma | Neuroendocrine | Advanced and Metastatic Silent Neuro-Endocrine Tumors | Non Functioning Neuroendocrine Tumors (NETs) | Non Syndromic Neuroendocrine Tumors | Carcinoids | Non Functioning

Sweden, Italy, Germany, United Kingdom, Spain, France, Netherlands, Poland
Nantes University Hospital
Nantes Genomics platform

Completed

Inter-regional Project of the Great Western Exploration Approach for Exome Molecular Causes Severe Intellectual Disability Isolated or Syndromic (HUGODIMS)

Severe Intellectual Disability

France
Assistance Publique Hopitaux De Marseille

Unknown

Antibiotic Stewardship in Infectious Disease Departement

Infectious Disease

France
RenJi Hospital

Unknown

Effects of Intraoperative Normal Saline vs Lactated Ringer on Outcomes in Pediatric Liver Transplantation

Biliary Atresia Intrahepatic Syndromic Form

China
Duke University
Foundation for Prader-Willi Research

Completed

Prader-Willi Syndrome Macronutrient Study

Childhood Obesity | Prader Willi Syndrome | Syndromic Obesity

United States, Canada
Assistance Publique - Hôpitaux de Paris

Completed

Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia (HCD GENE)

Isolated Non Syndromic Left CDH With Postero Lateral Diaphragmatic Defect With Good Perinatal Outcome

France
Northwestern University

Withdrawn

Novel Treatment for Syndromic Ichthyoses

CHILD Syndrome | Smith Lemli Opitz Syndrome | Syndromic Ichthyoses | Conradi Syndrome
Centre Hospitalier National d'Ophtalmologie des...
Institut National de la Santé Et de la Recherche Médicale, France

Unknown

Clinical and Genetic Examination of Usher Syndrome Patients' Cohort in Europe (EURUSH)

Usher Syndrome

France, Germany, Netherlands, Portugal
Assistance Publique - Hôpitaux de Paris

Completed

Epidemiology of Non-syndromic Dominant Deafness (SURDOM)

Hearing Impairment

France
University Hospital, Bordeaux

Completed

Microarray Analysis in Syndromic Obesity (REMOB)

Mental Retardation | Syndromic Obesity

France
French National Agency for Research on AIDS and...

Completed

Anti-Herpetic Treatment of Genital Ulcer : Effect on HIV & Herpes Shedding (ANRS 1212)

Ulcer | Herpes Genitalis

Central African Republic, Ghana
National Human Genome Research Institute (NHGRI)

Completed

Positional Cloning of the Gene(s) Responsible for Alagille Syndrome

Alagille Syndrome

United States

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