Clinical Trials : Pneumoconiosis

Recruiting

Study Name: A Study on Pneumoconiosis Treated With Whole-lung Lavage Combined With Mesenchymal Stem Cells
Condition: Pneumoconiosis
Date: 2016-01-20
Interventions:

Procedure: large volume whole-lung lavage (WLL)

Not yet recruiting

Study Name: Human Umbilical Cord-Mesenchymal Stem Cells for Pneumoconiosis
Condition: Pneumoconiosis
Date: 2016-05-20
Interventions: Biological: Human umbilical cord mesenchymal stem cells A single dose of 2×107 hUC-MSC will be impl

Recruiting

Study Name: Comprehensive Risk Assessment of People With Silicosis: A Population-based Study
Condition: Silicosis
Date: 2016-05-30
Interventions: Other: People with silicosis

Completed

Study Name: Safety Study of Autologous Bone Marrow Stromal Cells With Modification by Hepatocyte Growth Factor to Treat Silicosis
Condition: Silicosis
Date: 2013-10-30
Interventions: Other: Cells

Completed

Study Name: Oscillation Mechanics of the Respiratory System in Never-smoking Patients With Silicosis
Condition: Silicosis
Date: 2012-10-30

Completed

Study Name: Oxidative Stress Biomarkers to Monitor and Early Detect Health Impairment in Workers Exposed to Silica (Caesar Stone)
Condition: Silicosis
Date: 2011-02-06

Completed

Study Name: DNA-damage Pathways in Workers Exposed to Silica (Caesar Stone)
Condition: Silicosis
Date: 2011-02-06

Active, not recruiting

Study Name: Observational Study of Deferiprone (Ferriprox®) in the Treatment of Superficial Siderosis
Condition: Superficial Siderosis
Date: 2011-01-20

Completed

Study Name: Safety of Stem Cells Intrabronchial Instillation for Silicosis
Condition: Chronic and Accelerated Silicosis
Date: 2010-11-10
Interventions: Other: Autologous cell transplantation Intrabronchial Instillation Of Bone Marrow Derived Mononuclear Ce

Completed

Study Name: A Prospective Safety Follow Up Study Of Subjects Enrolled In Study A4321001 And Who Have Received Drug Product
Condition: Siderosis
Date: 2007-05-07
Interventions: Other: Observational Trial No intervention is being used in this study.

Search for Clinical Trial Results

Pneumoconiosis - 15 Studies Found

Status	Study
Recruiting	Study Name: A Study on Pneumoconiosis Treated With Whole-lung Lavage Combined With Mesenchymal Stem Cells Condition: Pneumoconiosis Date: 2016-01-20 Interventions: Procedure: large volume whole-lung lavage (WLL)
Not yet recruiting	Study Name: Human Umbilical Cord-Mesenchymal Stem Cells for Pneumoconiosis Condition: Pneumoconiosis Date: 2016-05-20 Interventions: Biological: Human umbilical cord mesenchymal stem cells A single dose of 2×107 hUC-MSC will be impl
Recruiting	Study Name: Comprehensive Risk Assessment of People With Silicosis: A Population-based Study Condition: Silicosis Date: 2016-05-30 Interventions: Other: People with silicosis
Completed	Study Name: Safety Study of Autologous Bone Marrow Stromal Cells With Modification by Hepatocyte Growth Factor to Treat Silicosis Condition: Silicosis Date: 2013-10-30 Interventions: Other: Cells
Completed	Study Name: Oscillation Mechanics of the Respiratory System in Never-smoking Patients With Silicosis Condition: Silicosis Date: 2012-10-30
Completed	Study Name: Oxidative Stress Biomarkers to Monitor and Early Detect Health Impairment in Workers Exposed to Silica (Caesar Stone) Condition: Silicosis Date: 2011-02-06
Completed	Study Name: DNA-damage Pathways in Workers Exposed to Silica (Caesar Stone) Condition: Silicosis Date: 2011-02-06
Active, not recruiting	Study Name: Observational Study of Deferiprone (Ferriprox®) in the Treatment of Superficial Siderosis Condition: Superficial Siderosis Date: 2011-01-20
Completed	Study Name: Safety of Stem Cells Intrabronchial Instillation for Silicosis Condition: Chronic and Accelerated Silicosis Date: 2010-11-10 Interventions: Other: Autologous cell transplantation Intrabronchial Instillation Of Bone Marrow Derived Mononuclear Ce
Completed	Study Name: A Prospective Safety Follow Up Study Of Subjects Enrolled In Study A4321001 And Who Have Received Drug Product Condition: Siderosis Date: 2007-05-07 Interventions: Other: Observational Trial No intervention is being used in this study.