Search clinical trials for: Genome analysis

Total 11180 results

Fondazione IRCCS Ca' Granda, Ospedale Maggiore...
Federico II University; Istituto Auxologico Italiano; Università degli Studi...

Recruiting

Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks

Beckwith-Wiedemann Syndrome

Italy
Yonsei University

Recruiting

A Prospective, Multi-center Clinical Study to Establish Multi-Cancer Early Detection Platform Through the Analysis of Whole Genome Sequencing of Circulating DNA in Cancer Patients and Healthy Volunteers

Healthy Volunteer | Invasive Cancer

Korea, Republic of
Vall d'Hebron Institute of Oncology

Recruiting

Predictive Biomarkers of Response to Checkpoint Inhibitors in Triple Negative Breast Cancer: a Multiomics Platform (PORTRAIT)

Triple Negative Breast Cancer

Spain
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
Shanghai Jiao Tong University School of Medicine
The First Affiliated Hospital of Nanchang University; The Affiliated Hospital... and other collaborators

Recruiting

Clinical Characteristics, Lifestyle and Multi-omics Analysis in Autoimmune Gastritis

Autoimmune Gastritis

China
Region Skane

Recruiting

BioMEL- Diagnostic and Prognostic Factors in Melanoma. (BioMEL)

Melanoma | Mutation | Image | Dysplastic Nevi | Melanoma in Situ | Mole (Dermatology)

Sweden
University Children's Hospital Basel

Recruiting

Early Pulmonary Dysfunction in Childhood Cancer Patients (SWISS-Pearl)

Pulmonary Dysfunction

Switzerland
Children's Oncology Group
National Cancer Institute (NCI)

Recruiting

Genetic Overlap Between Anomalies and Cancer in Kids in the Children's Oncology Group: The COG GOBACK Study

Pediatric Cancer | Congenital Anomaly

United States
Taipei Veterans General Hospital, Taiwan

Recruiting

To Evaluate the Short-term and Long Term Efficacy of Acupuncture in Ocular and Oral Dryness Symptoms of Dry Eye Syndrome

Dry Eye Syndrome | Xerophthalmia

Taiwan
University Hospital Tuebingen

Recruiting

Diagnostic Value of Exome/ Genome Sequencing, Conventional Methods in Rare Diseases and Familial Tumor Syndromes (EXGEFATU)

Rare Diseases | Genetic Predisposition

Germany
University Hospital Tuebingen

Recruiting

Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings

Genetic Predisposition to Disease | Rare Diseases

Germany
British Columbia Cancer Agency
Hoffmann-La Roche

Recruiting

Investigating the Effects of Atezolizumab in People Whose Tumour DNA or RNA Indicates Possible Sensitivity (CAPTIV-8)

Sarcoma | Breast Cancer | Head and Neck Cancer | Gynecologic Cancer | Lung Cancer | Skin Cancer | Gastrointestinal Cancer | Unknown Primary Tumors | Genitourinary Cancer

Canada
University Hospital, Basel, Switzerland
Swiss National Science Foundation

Recruiting

Development of a Swiss Surveillance Database for Molecular Epidemiology of Hypervirulent and Multi-drug Resistant Pathogens

Multiresistant Bacterial Pathogens | Virulent Bacterial Pathogens

Switzerland
Centre Hospitalier Universitaire Dijon

Recruiting

ANDDI-PRENATOME - Feasibility Study for a " Fast " Pangenomic High Throughput Sequencing Analysis in Prenatal Diagnosis (AnddiPrenatome)

Prenatal | Genome-wide High Throughput Sequencing

France
Imperial College London
Royal Brompton & Harefield NHS Foundation Trust; British Heart Foundation

Recruiting

Defining the Genetics, Biomarkers and Outcomes for Dilated Cardiomyopathy (Go-DCM)

Cardiovascular Diseases | Dilated Cardiomyopathy

United Kingdom
China National Center for Cardiovascular Diseases
Peking Union Medical College Hospital

Recruiting

Registration Study for Rare Type of Pulmonary Hypertension

Pulmonary Hypertension

China
St. Jude Children's Research Hospital

Recruiting

Familial Investigations of Childhood Cancer Predisposition (SJFAMILY)

Pancreatic Cancer | Hodgkin Lymphoma | Lynch Syndrome | Tuberous Sclerosis | Fanconi Anemia | AML | Non Hodgkin Lymphoma | Familial Adenomatous Polyposis | Acute Leukemia | Nevoid Basal Cell Carcinoma Syndrome | Neurofibromatosis Type 1 | Neuroblastoma | Retinoblastoma | MDS | Rhabdomyosarcoma | Von Hippel-Lindau Disease | Adrenocortical Carcinoma and other conditions

United States
University of Pittsburgh
Horizon Pharma USA, Inc.

Recruiting

Exome and Genome Analysis to Elucidate Genetic Etiologies and Population Characteristics in the Plain Community

Undiagnosed Disease

United States
Cervesi Hospital, Cattolica, Italy

Recruiting

Analysis of Human Genomic DNA in Embryo's Culture Media

Single-Gene Disease

Italy
National Human Genome Research Institute (NHGRI)

Recruiting

Use of Cysteamine in the Treatment of Cystinosis

Cystinosis

United States
National Human Genome Research Institute (NHGRI)

Recruiting

Analysis of Specimens From Individuals With Pulmonary Fibrosis

Pulmonary Fibrosis | Healthy Volunteers | Hermansky-Pudlak Syndrome (HPS)

United States
National Human Genome Research Institute (NHGRI)

Completed

Genetic Analysis of Attention Deficit Hyperactivity Disorder (ADHD)

ADHD

United States
IRCCS Eugenio Medea

Completed

Omic Approaches to Neurodevelopmental Disabilities

Neurodevelopmental Disorders

Italy
Vanda Pharmaceuticals

Completed

WGS Analysis of COVID-19 Positive Patients (CALYPSO)

COVID-19 | Coronavirus Infection

United States
International Medical University
Merck Sharp & Dohme LLC; University of Malaya; University of Southampton; Universiti... and other collaborators

Active, not recruiting

Paediatric Pneumococcal Pneumonia in Malaysia Prior to and During Pneumococcal Conjugate Vaccine (PCV) Implementation (MSIP PCV)

Pneumonia, Pneumococcal | Pneumonia Childhood

Malaysia
UNICANCER
AstraZeneca; Fondation ARC

Active, not recruiting

SAFIR02_Breast - Efficacy of Genome Analysis as a Therapeutic Decision Tool for Patients With Metastatic Breast Cancer (SAFIR02_Breast)

Metastatic Breast Cancer

France
Institut Curie

Completed

Pan-genome Analysis of Neuroblastoma by Comparative Genomic Hybridization and Correlation With Pathology for the Diagnostic and the Prognostic Classification (PHRCNB07)

Neuroblastoma

France
University Hospital Tuebingen

Completed

NGS Diagnostic in COVID-19 Hosts - Genetic Cause Relating to the Course of Disease Progression (COVID-19 NGS)

COVID-19

Germany
Jerry Vockley, MD, PhD

Enrolling by invitation

Genome Sequencing in the Intensive Care Unit Population (PISCES)

Genetic Disease | Infant, Newborn, Disease

United States
Matthew Milowsky, MD
Hoosier Cancer Research Network; Bladder Cancer Advocacy Network (BCAN®)

Completed

UC-GENOME: Urothelial Cancer-GENOmic Analysis to iMprove Patient Outcomes and rEsearch

Bladder Cancer | Urothelial Carcinoma | Urethral Cancer | Cancer of the Ureter

United States
Assistance Publique Hopitaux De Marseille

Completed

Identification of New Genetic Markers for the Risk of Recurrence of Venous Thromboembolism by Whole Genome Analysis (MARTHARecidive)

Venous Thromboembolism (VTE)

France
Assistance Publique Hopitaux De Marseille

Completed

Implementation of Innovative Techniques in Routine Diagnosis of Childhood Acute Leukemia: Analysis of Genome and Transcriptome by Micro-array

Acute Leukemia

France
The University of Hong Kong

Enrolling by invitation

Prospective Evaluation on Cognitive Function and Its Associated Genetic Vulnerability in Cannabis Users (SToP-C_PeCoG)

Cannabis Use | Neurocognitive Dysfunction | Genetic Predisposition

Hong Kong
University Hospital, Basel, Switzerland

Enrolling by invitation

Comparison of Pulsed-field Gel Electrophoresis and Whole Genome Sequencing to Determine Transmission Rate of ESBL-producing E.Coli (PFGE-WGS)

Analysis Transmission Rate

Switzerland
Asfendiyarov Kazakh National Medical University

Completed

The Role of Genetic Factors in the Development of Bronchial Asthma in the Kazakh Population

Bronchial Asthma | Genome Wide Association Studies

Kazakhstan
Janna Berg
Oslo University Hospital

Active, not recruiting

Identification of Predictive and Prognostic Markers for Lung Cancer With Metastases

Lung Cancer | Metastases | Primary Tumor

Norway
University Hospital Tuebingen

Completed

Whole Genome Trio Sequencing as a Standard Routine Test in Patients With Rare Diseases - "GENOME FIRST APPROACH"

Rare Diseases | Genetic Predisposition

Germany
Centre Hospitalier Universitaire Dijon

Completed

Study of the Diagnostic Value of "Rapid" High Throughput Genome Sequencing Analysis in Diagnostic Emergency Situations (FASTGEN)

Developmental Anomalies

France
National Human Genome Research Institute (NHGRI)

Completed

A Study of the Genetic Analysis of Brain Disorders

Holoprosencephaly

United States
Chinese University of Hong Kong

Completed

Genome-wide Analysis of Lipid-lowering Efficacy and Drug Level of Simvastatin and Rosuvastatin

Hypercholesterolemia

Hong Kong
University Hospital, Lille
University of Lausanne Hospitals; Seventh Framework Programme

Completed

Genetic Susceptibility Factors for Candidemia.

Candidemia | Genetic Predisposition to Disease | Invasive Candidiasis

France
British Columbia Cancer Agency
Genome British Columbia; BC Cancer Foundation

Unknown

Real-world Clinical Effectiveness of Whole Genome and Transcriptome Analysis to Guide Advanced Cancer Care

Metastatic Cancer | Advanced Cancer | Cancers That Cannot be Treated With Curative Intent
Assiut University

Unknown

Presentation, Clinical Course and Patterns of Myocardial Damage Due to Viral Myocarditis

Viral Myocarditis

Egypt
University Health Network, Toronto

Completed

Feasibility Clinical Study of Targeted and Genome-Wide Sequencing

Solid Tumors

Canada
National Human Genome Research Institute (NHGRI)

Completed

Genetic Analysis of Hereditary Prostate Cancer

Prostate Cancer

United States, Finland
National Human Genome Research Institute (NHGRI)

Completed

Genetic Analysis of Hereditary Non-Syndromic Oral Clefts

Hereditary Oral Clefts

Syrian Arab Republic
Medical College of Wisconsin
Children's Hospital and Health System Foundation, Wisconsin

Completed

Genetic Analysis of Children With Cyclic Vomiting Syndrome (CVS) and Migraines

Vomiting | Migraines

United States
National Human Genome Research Institute (NHGRI)

Completed

Analysis of Data From the Women's Contraceptive and Reproductive Experiences (CARE) Study

Breast Cancer

United States
St. Jude Children's Research Hospital

Completed

Genetic Study of Familial Acute Lymphoblastic Leukemia

Acute Lymphoblastic Leukemia (ALL)

United States
National Human Genome Research Institute (NHGRI)

Terminated

Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish Population

Hereditary Oral Clefts | Neural Tube Defects (NTDs) | Facial Cleft Defect

United States

Search clinical trials for: Genome analysis

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