Genotyping: Clinical Trials

9 trials of Genotyping, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

5 completed, 2 terminated, 1 unknown, 1 withdrawn. 9 Not applicable.

By phase and status

PhaseTrialsStatus
Not applicable9Completed 5, Terminated 2, Unknown 1, Withdrawn 1

Follow Genotyping: new trials by email Literature Review of Genotyping trials Research Report on Genotyping

Trials (filtered) newest first · largest first

All 9 trials

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Early Targeted Antibiotic Therapy in Patients With Sepsis
targeted antibiotics therapy - Sepsis
Not applicableCompletedRehab Werida482022-05-012023-09-28
Clinical Impact of Enhanced Risk Assessments in Women With a BRCA1/2 Mutation, CARE Study
Best Practice, Biospecimen Collection, Counseling - BRCA1/2-Associated Hereditary Breast and Ovarian Cancer Syndrome
Not applicableCompletedOhio State University Comprehensive Cancer Center1522018-01-012025-06-27
Impact of Genotyping P450 2C19 on Hospitalization Period
genotyping - Infection
Not applicableWithdrawnUniversity Hospital, Toulouse2016-12-012026-06-29
Human Genomic Population Structure and Phenotype-genotype Variation in ADME Genes in Four Populations
Phenotyping, Genotyping - Healthy
Not applicableCompletedEstella S. Poloni3672015-11-012017-05-10
Pharmacogenetic Prediction of Metoprolol Effectiveness
metoprolol succinate, Genotyping, CYP2D6 Phenotyping - Hypertension
Not applicableTerminatedUniversity of Colorado, Denver4622014-09-012021-09-16
Pharmacotoxicology of Trichloroethylene Metabolites
Dichloroacetate, Genotyping, Leucine - Healthy
Not applicableTerminatedUniversity of Florida22011-08-012015-06-03
LOC387715/HTRA1 Variants in Polypoidal Choroidal Vasculopathy in a Korean Population
LOC387715/HTRA1 genotyping - Age-Related Macular Degeneration
Not applicableCompletedKyungpook National University Hospital2152010-04-012011-08-30
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy
realization of a family tree, refractometry, evaluation of the presence of a nystagmus - Amaurosis, Retinal Diseases
Not applicableCompletedNantes University Hospital3602007-04-012011-11-24
Connexin Genotypes in Cystic Fibrosis
Genotyping, Lung function, Microbiology - Cystic Fibrosis, Inflammation
Not applicableUnknownUniversity Childrens' Hospital (Zentrum für Kinderheilkunde des Universitätsklinikum Bonn)3002002-04-012021-08-16

Conditions studied

Blindness (1)  ·  Camurati-Engelmann Syndrome (1)  ·  Cystic Fibrosis (1)  ·  Hereditary Breast and Ovarian Cancer Syndrome (1)  ·  Hypertension (1)  ·  Infections (1)  ·  Inflammation (1)  ·  Macular Degeneration (1)  ·  Mycoses (1)  ·  Retinal Diseases (1)  ·  Retinal Dystrophies (1)  ·  Sepsis (1)

Sponsors

Estella S. Poloni (1)  ·  Kyungpook National University Hospital (1)  ·  Nantes University Hospital (1)  ·  Ohio State University Comprehensive Cancer Center (1)  ·  Rehab Werida (1)  ·  University Childrens' Hospital (Zentrum für Kinderheilkunde des Universitätsklinikum Bonn) (1)  ·  University Hospital, Toulouse (1)  ·  University of Colorado, Denver (1)  ·  University of Florida (1)

Countries

United States (3)  ·  Czechia (1)  ·  Egypt (1)  ·  Ethiopia (1)  ·  France (1)  ·  Germany (1)  ·  Greece (1)  ·  Netherlands (1)  ·  Oman (1)  ·  South Korea (1)

Top investigators

Amanda E Toland (1)  ·  Andrew Monte, MD (1)  ·  Bernard Puech, MD (1)  ·  Carl Arndt, MD (1)  ·  Christian Hamel, MD (1)  ·  Christophe Orssaud, MD (1)  ·  Eman Momtaz (1)  ·  Emmanuel Bui Quoc, MD (1)  ·  Estella S. Poloni, Dr (1)  ·  In Taek Kim, M.D. (1)  ·  Michel Weber, MD (1)  ·  Noha Elbassiony (1)

Results publications

PMID 11834520, PMID 12525569, PMID 15579374, PMID 15955304, PMID 16183806, PMID 16622779, PMID 17099022, PMID 24062613, PMID 25301274, PMID 26009202, PMID 31768064, PMID 32160915, PMID 32274170, PMID 32851583, PMID 33193670, PMID 37525914, PMID 8166795

NIH funding

K23GM110516 (1), R01ES014617 (1)