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Disease Susceptibility clinical trials

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NCT ID: NCT02284295 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Molecular, Cytological Features and Genetic Susceptibility of COPD Attributable to Different Environmental Exposures 2

Start date: November 2014
Phase: N/A
Study type: Observational

The objective of this study is to investigate molecular, cytological and genetic features of occupational chronic obstructive pulmonary disease (COPD) in conditions of different occupational exposures. In order to achieve this goal serum pro-inflammatory cytokines and standard inflammation markers level, hemostasis, cytological analysis of bronchoalveolar lavage fluid and association of single nucleotide polymorphisms (SNPs) rs1800470 transforming growing factor β1 (TGF β1) gene, rs1828591 hedgehog interacting protein (HHIP) gene, rs4129267 interleukin 6 receptor (IL-6R) gene, rs1051730 nicotinic acetylcholine receptor 3 (CHRNA3) gene with COPD in subjects exposed to silica dust and in those exposed to polycyclic aromatic hydrocarbons exhaust will be investigated. The relationship between genotype and phenotype characteristics, such as an inflammation activity, assessed by C-reactive protein (hsCRP) and tumor necrosis factor alpha (TNF α) serum concentration, in different occupational COPD groups will be studied. The hypothesis is that the mechanisms underlying disease development and progression are different due to environmental risk factor that reflex in differs in disease attributes - molecular biomarkers, cytology results and genetic susceptibility between COPD due to dust, COPD due to chemicals and COPD in smokers therefore COPD can be subdivided into ecological phenotypes according to environmental risk factor.

NCT ID: NCT02220387 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Molecular, Cytological Features and Genetic Susceptibility of COPD Attributable to Different Environmental Exposures

Start date: August 2014
Phase: N/A
Study type: Observational

The objective of this study is to investigate molecular, cytological and genetic features of occupational chronic obstructive pulmonary disease (COPD) in conditions of different occupational exposures. In order to achieve this goal serum pro-inflammatory cytokines and standard inflammation markers level, hemostasis, cytological analysis of bronchoalveolar lavage and associations of single nucleotide polymorphisms (SNPs) rs1800470 transforming growing factor β1 (TGF β1) gene, rs1828591 hedgehog interacting protein (HHIP) gene, rs4129267 interleukin 6 receptor (IL-6R) gene, rs1051730 nicotinic acetylcholine receptor 3 (CHRNA3) gene with COPD in subjects exposed to silica dust and in those exposed to polycyclic aromatic hydrocarbons exhaust will be investigated. The relationship between genotype and phenotype characteristics, such as an inflammation activity, assessed by C-reactive protein (hsCRP) and tumor necrosis factor-α (TNF α) serum concentration, in different occupational COPD groups will be studied. The hypothesis is that the mechanisms underlying disease development and progression are different due to environmental risk factor that reflex in differs in disease attributes - molecular biomarkers, cytology results and genetic susceptibility between COPD due to dust, COPD due to chemicals and COPD in smokers therefore COPD can be subdivided into ecological phenotypes according to environmental risk factor.

NCT ID: NCT02212964 Completed - Radiation Injury Clinical Trials

Differentiation of Pseudoprogression and True Progression Through High Field Susceptibility Weighted Imaging and R2*

Start date: July 2014
Phase: N/A
Study type: Observational

Using a multi-echo gradient echo sequence to calculate R2* and quantitative susceptibility maps and well as susceptibility-weighted imaging post processing the investigators hypothesize that the investigators would be able to distinguish between pseudoprogression and true progression with the use of an easily implementable sequence on clinical MRI scanners.

NCT ID: NCT02190214 Completed - Hypothyroidism Clinical Trials

Thyroid Disorders in Malaysia: A Nationwide Multicentre Study

MyEndo-Thyroid
Start date: August 2014
Phase: N/A
Study type: Observational

This will be a population based study looking at the prevalence of thyroid disorders in Malaysia (including hypo- and hyperthyroidism, subclinical hypo- or hyperthyroidism) and its association with different ethnicity and iodine status. The study will also look at genetic susceptibility for autoimmune thyroid disorders in the Malaysian population General hypotheses: The prevalence of thyroid disorders in Malaysia is 10% for hypothyroidism and 2% for hyperthyroidism Hypo- and hyperthyroidism is associated with iodine status in our population There are different susceptibility gene for autoimmune thyroid disorder in different ethnicity in our population

NCT ID: NCT02188862 Completed - Clinical trials for Rheumatic Heart Disease

Genetic Susceptibility to Rheumatic Heart Disease in the Pacific Region

Start date: September 2012
Phase: N/A
Study type: Observational

The purpose of this study is to investigate whether there are genetic differences between patients with rheumatic heart disease and members of the general population.

NCT ID: NCT02134496 Completed - Clinical trials for Osteoarthritis Susceptibility 3

PACU Discharge Without Motorfunction Assessment After Spinal Anaesthesia

Start date: June 2014
Phase: N/A
Study type: Interventional

The study investigates the safety of discharge from the Post-Anesthesia Care Unit (PACU) without assessment of motorfunction after spinal anesthesia for total hip- or knee replacement. This is an randomized controlled trial between two groups with assessment of normal (Aldrete) PACU discharge criteria with or without assessment of the motorfunction. The study hypothesis is that it is safe to be discharged from the PACU to a ward without assessment of motor function. The main outcome is length of hospial stay (LOS) in days and re-admission within the first 30 days after surgery . Secondary outcomes include adverse events up to 24 hours after surgery, and minuttes spent in the PACU after surgery. Participants will be monitores for adverse events for the first 24 hours after surgery and reported. The total number of minuttes spent in the PACU will be recorded and reported.

NCT ID: NCT02120638 Recruiting - Clinical trials for Multidrug Resistant Tuberculosis

Optimization of MDR-TB Treatment Regimen Based on the Molecular Drug Susceptibility Results of Pyrazinamide

Start date: April 2014
Phase: Phase 3
Study type: Interventional

Multidrug resistant tuberculosis (MDR-TB) is difficult to treat and raises a great challenge to TB control program. That pyrazinamide can shorten the course of treatment and facilitate bacilli clearance has been proved recently. In 2011, WHO recommended to use pyrazinamide throughout the course of treatment for MDR-TB. However, pyrazinamide susceptibility testing has not been widely used in clinic. And the conventional testing is time-consuming and unreliable. In contrast, the detection of pncA and rpsA mutations with molecular methods can provide rapid results of pyrazinamide susceptibility. The purpose of this study is to evaluate the efficacy of the introduce the molecular testing of pyrazinamide susceptibility in optimizing the MDR-TB treatment regimen.

NCT ID: NCT02084030 Recruiting - Clinical trials for Cardiac Surgery Patients

Screening of Susceptibility Genes in Postoperative Cognitive Dysfunction(POCD)

Start date: March 2013
Phase: N/A
Study type: Observational

The aim of this study is to perform a whole-genome linkage analysis for identification of the susceptibility loci for POCD

NCT ID: NCT02056938 Terminated - Clinical trials for Kidney Transplantation

ATG Versus Basiliximab in Kidney Transplant Displaying Low Immunological Risk But High Susceptibility to DGF

PREDICT-DGF
Start date: June 2014
Phase: Phase 4
Study type: Interventional

The primary objective of the following randomized open label trial is to demonstrate how low immunological risk patients (no anti HLA immunization and first kidney transplantation) but diagnosed at high-risk of delayed graft function (assessed by DGFS score) could benefit from induction with ATG for preventing delayed graft function compared to Basiliximab.

NCT ID: NCT02053805 Recruiting - Lynch Syndrome Clinical Trials

Prostate Cancer Screening Among Men With High Risk Genetic Predisposition

Start date: February 2014
Phase: N/A
Study type: Interventional

This will be a prospective diagnostic trial of screening for prostate cancer among men with genetic predisposition.