Genetic Disorder Clinical Trial
Official title:
Molecular Typing of Adult Community-acquired Pneumonia in China
Community-acquired pneumonia (CAP) is a heterogeneous disease causing great morbidity,
mortality and health care burden globally. Typing methods for discriminating different
clinical conditions of the same disease are essential to a better management of CAP.
Traditional typing systems based separately on clinical manifestations (such as PSI and
CURB-65), pathogens(bacterial types, virulence, drug resistance, etc) or host immune state
(immunocompetent, immunocompromised or immunodeficiency). Thus, they are barely able to
represent the real disease status nor to precisely predict the mortality.
As the development of multi-omic technologies, the relatedness of different phenotypes at a
molecular level have revolutionized our ability to differentiate among patients. Our study
is aimed at establishing a novel molecular typing method of CAP. Multi-omic (including
genomics, transcriptomes, and metabolisms) data obtained from enrolled CAP patients and
isolated pathogens would be integrated analyzed and interpreted. Tthe investigators believe
that an appropriate molecular typing method would lead to revolutionary changes in current
arrangements of CAP.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01734486 -
Growth Response in Girls With Turner Syndrome
|
Phase 4 | |
Completed |
NCT01529944 -
Genetic Testing of Noonan Subjects Previously Treated With Norditropin®. An Extension to Trial GHNOO-1658
|
Phase 3 | |
Completed |
NCT01518036 -
Use of Somatropin in Turner Syndrome
|
Phase 3 | |
Completed |
NCT00025870 -
Studies of Children With Metabolic and Other Genetic Disorders
|
||
Completed |
NCT01563926 -
Evaluating Acceptance of New Liquid Somatropin Formulation in Children With Growth Hormone Deficiency
|
Phase 3 | |
Active, not recruiting |
NCT01851447 -
Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular Dystrophy
|
||
Completed |
NCT01435629 -
A Survey Collecting Data on Adult Height in Patients With Achondroplasia Treated With Somatropin
|
N/A | |
Completed |
NCT01245374 -
Norditropin NordiFlex® Device Compared to the Device Previously Used by Patients or Parents
|
Phase 4 | |
Terminated |
NCT01135537 -
Pharmacokinetics of Thymoglobulin in Paediatric Haematopoietic Stem-cell Transplants
|
Phase 2 | |
Completed |
NCT00705172 -
Retrospective Observational Study on Efficacy and Safety of Norditropin® in Children With Prader-Willi Syndrome
|
||
Completed |
NCT01518062 -
Safety of Somatropin and Induction of Puberty With 17-beta-oestradiol in Girls With Turner Syndrome
|
Phase 4 | |
Recruiting |
NCT02769949 -
Pediatric Patients With Metabolic or Other Genetic Disorders
|
||
Terminated |
NCT00358657 -
Fludarabine Phosphate, Cyclophosphamide, and Total-Body Irradiation Followed by Donor Bone Marrow Transplant and Cyclophosphamide, Mycophenolate Mofetil, Tacrolimus, and Sirolimus in Treating Patients With Primary Immunodeficiency Disorders or Noncancerous Inherited Disorders
|
Phase 2 | |
Completed |
NCT01604161 -
Non-interventional Study of Patients Using Norditropin® for Growth Hormone Deficiency or Turner Syndrome
|
N/A | |
Completed |
NCT01516229 -
Special Survey for Long Term Application
|
N/A | |
Enrolling by invitation |
NCT04681781 -
SLC13A5 Deficiency Natural History Study - Remote Only
|
||
Completed |
NCT01529840 -
Somatropin Effect on Linear Growth and Final Height in Subjects With Noonan Syndrome
|
Phase 3 | |
Completed |
NCT01710696 -
Induction of Puberty With 17-beta Estradiol in Girls With Turner Syndrome
|
Phase 3 | |
Completed |
NCT01401244 -
Bioequivalence of Two Somatropin Products (Norditropin® Versus Genotropin®) in Healthy Adult Volunteers
|
Phase 1 | |
Recruiting |
NCT05737602 -
Promoting Stress Management and Resilience Among Individuals With Von Hippel- Lindau Disease
|
N/A |