Search clinical trials for: Genetic analysis

Total 28156 results

Institut de Myologie, France
Association Française contre les Myopathies (AFM), Paris

Not yet recruiting

Natural History Study of Children With LAMA2-related Dystrophies (LAMA2)

Merosin Deficient Congenital Muscular Dystrophy

France
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
GENGE

Recruiting

GENETIC VARIABILITY TO GLP1 TREATMENT (GLP1 treatment)

Obesity | Type 2 Diabetes

Israel
ASST Fatebenefratelli Sacco

Not yet recruiting

Clonal Hematopoiesis in Giant Cell Arteritis (CH-GCA)

Giant Cell Arteritis | Temporal Arteritis | Clonal Hematopoiesis of Indeterminate Potential | Horton Disease | Systemic Vasculitis Primary
Eye & ENT Hospital of Fudan University
Shanghai Rehabilitation Institute for the Exceptional Children

Not yet recruiting

A Comparative Analysis of Speech Perception Between Cochlear Implant Patients and DFNB9 Patients Receiving Gene Therapy

Hearing Loss | Genetic Disease | Speech Perception

China
Gene Solutions

Recruiting

Analysis of PD-L1, TMB, MSI and ctDNA Dynamics to Predict and Monitor Response to Immunotherapy in Metastatic Cancer.

Breast Cancer | Gastric Cancer | Colorectal Cancer | Non Small Cell Lung Cancer | Advanced Cancer | Liver Cancer | Immune Checkpoint Inhibitor

Vietnam
Papworth Hospital NHS Foundation Trust
Innovate UK; Cystic Fibrosis Trust; US Cystic Fibrosis Foundation

Recruiting

Analysis of Remote Monitoring/Virtual Clinic Data in Adult Patients With Cystic Fibrosis (Project Breathe)

Cystic Fibrosis

United Kingdom
Fondazione Policlinico Universitario Agostino Gemelli...

Not yet recruiting

Hyperlactacidemia in Major Abdominal Surgery and Monocarboxylate Receptors (NETTUNO)

Postoperative Complications | Surgical Procedure, Unspecified | Hyperlactatemia | Abdomen Disease

Italy
University Hospital, Strasbourg, France

Recruiting

Identification of Y Chromosome From Free Circulating DNA in Patients With Turner Syndrome (Turner-Ylc)

Turner Syndrome

France
Chiesi Farmaceutici S.p.A.

Not yet recruiting

Analysis of Velmanase Alfa (Lamzede®)'s Effects in the Body of Children With Alpha-Mannosidosis Under the Age 3 (LAMPO(0-3))

Alpha-Mannosidosis
Sixth Affiliated Hospital, Sun Yat-sen University

Recruiting

Multicenter Analysis of Genomic and Metabolic Data of Neonatal Genetic Diseases (MAOFGAMDNGD)

Hereditary Diseases

China
Assistance Publique - Hôpitaux de Paris

Not yet recruiting

Study of the Blood and Skin Immunological Profile of Patients With Recessive Dystrophic Epidermolysis Bullosa: in Vivo Analysis and the Impact of Placental Stem Cells in Vitro (ISTRADEB)

Epidermolysis Bullosa Dystrophica
Gene Solutions

Recruiting

Analysis of Circulating Tumor DNA Dynamics to Predict and Monitor Response to TKI in Patients With Advanced NSCLC.

Non Small Cell Lung Cancer | Stage IIIB Non-small Cell Lung Cancer | Stage IV Non-small Cell Lung Cancer | Stage IIIC Non-Small Cell Lung Cancer | Tyrosine Kinase Inhibitors

Vietnam
University of Bonn

Recruiting

Characteristics of Hypophosphatasia in Adult Patients in Rheumatology (COHIR)

Hypophosphatasia

Germany
IRCCS San Raffaele

Not yet recruiting

WEST-KOaST Study: WES Analysis of Testicular Cancer Patientsand Their First-degree Family Members (West-KOaSt)

Testicular Cancer
IRCCS San Raffaele

Recruiting

Liquid Biospy for Urinary Cancers (CIRCE)

Urothelial Carcinoma

Italy
Igenomix

Recruiting

International Non-selection Study for ERA® Test in Patients With Previous Implantation Failures

Infertility of Uterine Origin | Implantation Failure

Brazil, Spain, Peru, United Kingdom, United States, Panama
University of Southern California
National Cancer Institute (NCI)

Recruiting

Confronting Cancer as a Community

Colorectal Carcinoma

United States
Sohag University

Recruiting

Angiotensin Converting Enzyme rs (1799752) Gene Polymorphism and Development of In-Stent Restenosis in Patients With Stable Coronary Artery Diseases in Sohag Hospital University.

Angiotensin Converting Enzyme rs (1799752) Gene Polymorphism and Development of In-Stent Restenosis in Patients With Stable Coronary Artery Diseases

Egypt
National Cancer Institute (NCI)

Recruiting

Adding an Immunotherapy Drug, MEDI4736 (Durvalumab), to the Usual Chemotherapy Treatment (Paclitaxel, Cyclophosphamide, and Doxorubicin) for Stage II-III Breast Cancer

Anatomic Stage II Breast Cancer AJCC v8 | Anatomic Stage III Breast Cancer AJCC v8 | Hormone Receptor-Positive Breast Carcinoma | HER2-Negative Breast Carcinoma

United States
Ruijin Hospital

Not yet recruiting

Real-World Study of DLBCL With Different Genetic Subtypes

Lymphoma | DLBCL - Diffuse Large B Cell Lymphoma

China
Memorial Sloan Kettering Cancer Center

Recruiting

A Study of Selinexor in People With Wilms Tumors and Other Solid Tumors

Solid Tumor | Rhabdoid Tumor | Wilms Tumor | Nephroblastoma | Malignant Peripheral Nerve Sheath Tumors | MPNST | XPO1 Gene Mutation

United States
University of Nottingham
Imperial College London; University of Leeds; Vanderbilt University Medical Center and other collaborators

Recruiting

Understanding Gut Symptoms in People With Cystic Fibrosis (GRAMPUS-CF SRC)

Cystic Fibrosis | Gastrointestinal Dysfunction

United Kingdom
Military University Hospital, Prague

Recruiting

Innovative Approach to Detect Recurrent Colorectal Lesions With Surveillance Via Mutation Analysis & Clinical Phenotype (MTG)

Predictive Cancer Model

Czechia
Fondazione Policlinico Universitario Agostino Gemelli...

Recruiting

Morphological, Genetic and Tumour Microenvironment Characterisation in Uveal Melanoma (MicroGenUM)

Uveal Melanoma

Italy
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
Institut de Myologie, France
Roche Pharma AG

Not yet recruiting

Home Monitoring of Adult Patients With SMA: a Pilot Multicenter Validation Study (SMA-AtHome)

Muscular Atrophy, Spinal, Type II | Muscular Atrophy, Spinal, Type III

France
Hugo W. Moser Research Institute at Kennedy Krieger...

Recruiting

Behavioral Assessment and Treatment of Problem Behavior in Children With Cornelia de Lange Syndrome

Cornelia de Lange Syndrome

United States
Qianfoshan Hospital

Recruiting

Analysis of the Effect of Iron Supplements on Iron Deficiency Anemia in Pregnancy

Iron Deficiency Anemia of Pregnancy | Iron Storage Disease

China
Fondazione Policlinico Universitario Agostino Gemelli...

Recruiting

FASHION Fabry Disease Hypertrophic Cardiomyopathy and Infammation (FASHION)

Fabry Disease

Italy
Mayo Clinic

Recruiting

Adding a Genetic Risk Evaluation to Standard Breast Cancer Risk Assessment for African American and Hispanic Women

Breast Carcinoma | Breast Atypical Ductal Hyperplasia | Breast Atypical Lobular Hyperplasia | Breast Lobular Carcinoma In Situ

United States
Centre Hospitalier Universitaire de Saint Etienne
Kyoto University, Graduate School of Medicine

Not yet recruiting

Analysis of the Genotype/Phenotype Relationship in the Fuchs' Corneal Endothelial Dystrophy in France (F3S2)

Corneal Dystrophies

France
University Hospital, Basel, Switzerland

Recruiting

Genetic Architecture of Neutrophil-Mediated Inflammatory Skin Diseases (NEUTROSKIN)

Inflammatory Dermatoses | Neutrophil-mediated Inflammatory Dermatoses

Switzerland
IRCCS Policlinico S. Donato
University of Milan

Recruiting

Analysis of Muscular Properties in Patients With MFS and EDS (MUSCLE)

Marfan Syndrome | Rare Diseases | Ehlers-Danlos Syndrome

Italy
University of Chicago

Recruiting

Hidradenitis - an Analysis of Genetic Traits and Linkages in Families

Hidradenitis Suppurativa

United States
Samara State Medical University

Recruiting

Clinical and Diagnostic Significance of Endothelial Dysfunction and Myocardial Contractility in Patients With AML

Endothelial Dysfunction | Cardiotoxicity | Acute Myeloid Leukemia, Adult

Russian Federation
IRCCS Policlinico S. Donato

Recruiting

Transcriptomic Study of Adult Population With Marfan Syndrome (MaRfaNomicA)

Marfan Syndrome | Marfan's Syndrome With Cardiovascular Manifestations

Italy
Pfizer

Recruiting

A Study to Understand the Long-term Safety and Effects of an Experimental Gene Therapy for Duchenne Muscular Dystrophy.

Duchenne Muscular Dystrophy

United States
University Children's Hospital, Zurich

Recruiting

Ureagenesis Analysis in Healthy Subjects and in Urea Cycle Disorder Patients

Urea Cycle Disorders

Switzerland
Menarini Biomarkers Singapore

Recruiting

Fetal Cell Analysis From Maternal Blood

Pregnancy Related | Genetic Disease | Prenatal Screening

Italy
University of Milano Bicocca

Recruiting

Candidate Gene for Hyperferritinemia (HyFerr)

Hyperferritinemia

Italy
Institute of Health Information and Statistics...
Centre of Cardiovascular and Transplantation Surgery, Czech Republic; The Central... and other collaborators

Recruiting

Pilot Project of Familial Hypercholesterolemia Screening in Newborns in the Czech Republic (CzeCH-IN)

Familial Hypercholesterolaemia

Czechia
Augusta University

Recruiting

Genetic Testing in African Americans (GTM-I)

Ovarian Cancer | Endometrial Cancer | Peritoneal Cancer

United States
Azienda Ospedaliero-Universitaria Careggi
University of Florence; Fondazione Don Carlo Gnocchi Onlus; Scuola Superiore...

Recruiting

PRedicting the EVolution of SubjectIvE Cognitive Decline to Alzheimer's Disease With Machine Learning (PREVIEW)

Alzheimer Disease | Mild Cognitive Impairment | Cognitive Decline

Italy
Hospital Garcia de Orta
Instituto de Medicina Molecular João Lobo Antunes

Recruiting

Diastolic Dysfunction in Septic Shock and Cardiomyopathy Genetic Variants (SepticHeartG)

Septic Shock | Cardiomyopathies | Diastolic Dysfunction

Portugal
RenJi Hospital
Peking University First Hospital; Shanghai Zhongshan Hospital; First Affiliated... and other collaborators

Recruiting

Frequency, Clinical Phenotype and Genetic Analysis of Heritable Kidney Cancer Syndromes

Kidney Cancer | Renal Cell Carcinoma | ALK Gene Mutation | MET Gene Mutation | HLRCC | Renal Tumor Histology | Cutaneous Leiomyoma | BAP1 Tumor Predisposition Syndrome | VHL Syndrome | Birt-Hogg-Dube Syndrome | Familial Renal Cancer | FLCN Gene Mutation | FH Gene Mutation | Cutaneous Leiomyomata With Uterine Leiomyomata

China
Maastricht University Medical Center

Recruiting

PCSK9 Polymorphism and Risk of Cardiac Rupture

Post-Infarction Heart Rupture | Gene Polymorphism

Italy
Chang Gung Memorial Hospital
Taipei Veterans General Hospital, Taiwan; Taipei Medical University; National...

Not yet recruiting

Effects of a Mixed Chinese Herbal Formula on Atopic Dermatitis

Atopic Dermatitis
Region Skane

Recruiting

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

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

Sweden
Shanghai Vitalgen BioPharma Co., Ltd.

Not yet recruiting

Lead-in Study of VGB-R04 Gene Therapy for Hemophilia B-- An Observational Survey Analysis Study

Hemophilia B

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