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NCT ID: NCT02509364 Enrolling by invitation - Clinical trials for Interstitial Lung Diseases

Study of the Etiology and Immunological Pathogenesis in Acute Exacerbation of Idiopathic Pulmonary Fibrosis (AE-IPF)

Start date: August 2015
Phase: N/A
Study type: Observational

Idiopathic pulmonary fibrosis (IPF) is a highly heterogeneous and lethal pathological process with limited therapeutic options, which is the most common and severe of the idiopathic interstitial pneumonias (IIPs). During the past 20 years, the incidence of IPF increased significantly. Most of IPF patients show a median survival time of 2-3 years after diagnosis. Five-year survival rate is 30%-50%. It's difficult to diagnose in the early stage of IPF. Once the patients go to hospital, it's already in the late stage. Now there is no effective therapy except lung transplant for IPF in clinical application. Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is a fatal condition with high mortality (over 80%). Its etiology and pathogenesis remain unknown. There is a lack of effective treatment for it. Based on the investigators' long-term clinical observation, most cases of AE-IPF initially got "common cold" and had coryza, more cough, nasal obstruction,rhinorrhea, sore throat, some patients had fever, headache, and etc. Some of these patients' condition developed very rapidly and then became very severe similar to the situation of acute respiratory distress syndrome (ARDS). Why these AE-IPF patients were so hypersensitive to "cold"? What were the immunologic and pathological mechanisms of their lung lesions after patients exposed to "common cold"? How to effectively offer interventional treatment for AE-IPF? All the above questions are yet to be explained clearly. In the investigators' previous retrospective study, the investigators found that there were some obviously imbalanced immune responses in IPF patients, including increased cluster of differentiation 4 (CD4) T cell population, immunoglobulin and complements. The investigators also found highly expressed inflammatory cytokines (IL-17, MIG and IL-9) and high detection rates of pathogens in AE-IPF patients, especially serum immunoglobulin M (IgM) antibody of some respiratory virus. These findings provide a strong suggestion that there are some imbalance of immunologic function in IPF and there are relationship between AE-IPF and infection, especially "Cold" virus infection might be a key trigger for AE-IPF.

NCT ID: NCT02462356 Enrolling by invitation - Clinical trials for Non Small Cell Lung Cancer

Multiple-portal VATS Versus Uniportal VATS Lobectomy for Non-small Cell Lung Cancer

MVUVLC
Start date: December 2015
Phase: N/A
Study type: Interventional

This study evaluate multiple-portal VATS and uniportal VATS lobectomy for NSCLC, half of participants will receive multiple VATS, while the other half will receive uniportal VATS lobectomy.

NCT ID: NCT02462304 Enrolling by invitation - Clinical trials for Diabetic Macula Edema

To Compare Anti-VEGF Monotherapy With Anti-VEGF and EPM Grid Laser Combination Therapy for Diabetic Macular Edema

END-DME
Start date: June 2015
Phase: Phase 4
Study type: Interventional

Objectives: To compare the efficacy of monotherapy with anti-Vascular Endothelial Growth Factor (ranibizumab or bevacizumab) with combined therapy with anti-Vascular Endothelial Growth Factor and end-point-management grid laser photocoagulation for diabetic macular edema. Study design: Open-label non-randomized interventional study. Study overview: This study aims to look at the efficacy of treating diabetic macular edema (DME) with either anti-Vascular Endothelial Growth Factor(anti-VEGF) monotherapy, compared with combination therapy with anti-VEGF and End-Point-Management (EPM) grid laser photocoagulation, over a period of 6 months. Various sites from across Asia (Japan, South Korea, Hong Kong) will participate. Depending on the availability of EPM laser, sites can either contribute to the 'Anti-VEGF monotherapy' arm, or to the 'Combination therapy' arm.

NCT ID: NCT02449356 Enrolling by invitation - Clinical trials for Mechanical Ventilation Complication

Clinical Study of the Endotracheal Tube Used in Prone Position Ventilation Condition

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

In this study, the investigators adopt the special endotracheal tube to those patients at prone posture during the operation,or those with acute respiratory distress syndrome in ICU, so that the investigators can reduce, or even avoid some severe complications during perianesthesia, and that the investigators can provide strong safeguard measures for the respiratory therapy of critical patients in ICU.

NCT ID: NCT02414802 Enrolling by invitation - Venous Thrombosis Clinical Trials

Study of a Novel Thrombectomy Device to Treat Acute Iliofemoral Deep Venous Thrombosis

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

The purpose of this study is to determine whether the novel aspiration thrombectomy device combined with catheter-directed thrombolysis is effective in the treatment of acute iliofemoral deep venous thrombosis (IF-DVT).

NCT ID: NCT02413060 Enrolling by invitation - Diabetes Clinical Trials

The Impact of Resistance Training on Type 2 Diabetes Patients.

Start date: March 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the long-term effects of high-intensity progressive resistance training could improve glucose and lipid metabolism in chinese type 2 diabetes.

NCT ID: NCT02365077 Enrolling by invitation - Femur Head Necrosis Clinical Trials

GWAS Identified Susceptibility Loci for Glucocorticoid-induced FHN in the Chinese Population

Start date: January 1, 2015
Phase:
Study type: Observational [Patient Registry]

This is a observation clinical trial. We are collecting the patients with glucocorticoid. They were divided into the experiment group (with femur head necrosis) and control group (without femur head necrosis).Then, we will analyse the patients' genome with genome-wide association study (GWAS). Our purpose is to find susceptibility loci for glucocorticoid-induced femur head necrosis in the Chinese population.

NCT ID: NCT02352077 Enrolling by invitation - Spinal Cord Injury Clinical Trials

NeuroRegen Scaffold™ With Stem Cells for Chronic Spinal Cord Injury Repair

Start date: January 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of NeuroRegen scaffold with bone marrow mononuclear cells (BMMCs) or mesenchymal stem cells (MSCs) in patients with chronic spinal cord injury.

NCT ID: NCT02325596 Enrolling by invitation - Rhinosinusitis Clinical Trials

Investigate the Role of microRNA in Chronic Rhinosinusitis From DC-Th Axis

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

This study aimed to evaluate the upstream events of Th17/Treg imbalance in CRS and their immune regulatory factors. Then the investigators aimed to explore the regulatory role of miRNA on DC-Th axis and its dysfunction in the pathogenesis of CRS, in order to determine the miRNA expression profile in CRS and clarify the role of miRNA in the pathogenesis of CRS by regulating the DC-Th axis.

NCT ID: NCT02307994 Enrolling by invitation - Oligospermia Clinical Trials

Clinical Research on Effectiveness and Safety of Treatment of Severe Oligospermia or Azoospermia With uFSH

Start date: August 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether uFSH is effective and safe in the treatment of male patients with severe oligospermia or azoospermia.