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Lung Diseases, Interstitial clinical trials

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NCT ID: NCT02370693 Completed - Systemic Sclerosis Clinical Trials

Comparing and Combining Bortezomib and Mycophenolate in SSc Pulmonary Fibrosis

Start date: March 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to look at whether bortezomib, mycophenolate or the combination of both is better to treat scarring of the lung caused by Systemic Sclerosis.

NCT ID: NCT02251964 Completed - Clinical trials for Lung Diseases, Interstitial

Rituximab in Interstitial Pneumonitis

RITUX-IP
Start date: September 2014
Phase: Phase 2/Phase 3
Study type: Interventional

This project will address rare immune mediated inflammatory diseases (IMIDs) involving the lungs, i.e. interstitial pneumonitis (IP). The main objective of this study is to assess the effects of rituximab (RTX) as a rescue therapy for progressive IMID-IP patients. The primary study parameter is pulmonary function. The secondary objectives are to explore the application of imaging with radiolabeled RTX as early predictor for efficacy of RTX, to study the effects of RTX treatment on quality of life, and to further elucidate the pathophysiology of IMID-IP by analyzing biochemical markers.

NCT ID: NCT02246023 Completed - Lung Cancer Clinical Trials

Fractionated Versus Target-controlled Propofol Administration in Bronchoscopy

Start date: January 2015
Phase: Phase 4
Study type: Interventional

After randomization, the subjects undergo flexible bronchoscopy either with fractionated propofol administration or with propofol-TCI. Measurement of blood pressure, heart rate, oxygen saturation, and oxygen requirement are measured continuously during the procedure and thereafter. Cumulative propofol dose, and induction, procedure, and recovery time are noted continuously during and after the procedure.

NCT ID: NCT02229994 Completed - Clinical trials for Cystic Fibrosis of the Adult

Development of a New Tool for Dyspnea Measurement in Chronic Respiratory Diseases

DYSLIM
Start date: March 16, 2010
Phase: N/A
Study type: Observational

The purpose of this study is the psychometric validation of a self-administered dyspnea questionnaire, usable in clinical practice in order to assess dyspnea and its impact on patients with chronic respiratory diseases.

NCT ID: NCT02201654 Completed - Clinical trials for Interstitial Lung Disease

Stylet vs No Stylet During EBUS TBNA

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

This research study compares two ways to biopsy lymph nodes in the chest using endobronchial ultrasound-guided transbronchial needle aspiration" (EBUS-TNBA). During a EBUS-TBNA procedure, the patient is sedated, and a flexible camera and ultrasound probe is inserted through the mouth into the large airways of the chest, allowing us to see (via ultrasound) and biopsy the lymph nodes in the chest. The purpose of this research study is to determine if the EBUS-TBNA procedure can be made simpler. In today's practice, the biopsy needle has two parts, 1) the needle itself and 2) an inner stylet that runs through the middle of the needle. Because many other biopsy needles (such as the needles used in breast biopsy and different types of lung biopsy needles) do not use an inner stylet, the investigators do not think the use of a stylet is necessary. If this step can be safely eliminated without decreasing the effectiveness of the procedure, this could shorten the procedure (saving time). This study is deigned to formally test the hypothesis that a stylet is not necessary in EBUS-TBNA.

NCT ID: NCT02197364 Completed - Clinical trials for Interstitial Lung Disease

The Role of KL-6 in the Clinical Diagnosis of ILD

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

The purpose of the study is to evaluate the significance of KL-6 as a biomarker in the clinical diagnosis of interstitial lung disease (ILD) by detecting serum KL-6 levels among patients with ILD, and comparing them to the clinical diagnostic criteria and other respiratory diseases. In addition, the study discusses the value of KL-6 levels in terms of ILD treatment effect evaluation through the detection of serum KL-6 levels before treatment and after treatment.

NCT ID: NCT02159651 Completed - Clinical trials for Interstitial Pneumonia Associated With Polymyositis/Dermatomyositis

A Survey for Long-term Use of Prograf Capsules in Patient With Interstitial Pneumonia

Start date: April 1, 2014
Phase:
Study type: Observational

This study is to evaluate the safety and the efficacy of Prograf in patients with interstitial pneumonia associated with polymyositis / dermatomyositis in acute clinical setting.

NCT ID: NCT02143687 Completed - Clinical trials for Interstitial Lung Disease

Patients With Pulmonary Hypertension or Interstitial Lung Disease at Altitude - Effect of Oxygen on Exercise Performance

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

The purpose of this study is to investigate the effect of travelling to moderate altitude and of nocturnal oxygen therapy during a stay at moderate altitude on exercise performance of patients with pulmonary hypertension or with interstitial lung disease.

NCT ID: NCT02125916 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Evaluating the Effect of Oxygentherapy on Concentration at Chronic Lung Patients

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

The objective is to study the cognitive functions in patients with chronic obstructive lung disease (COLD) and patients with interstitial lung disease (ILD) compared to healthy controls. The cognitive functions are tested with and without oxygen therapy to clarify the effect of oxygen therapy. Driving simulations is used to test the cognitive functions. The hypothesis is that patients with chronic lung disease have decreased cognitive functions and that oxygen therapy will increase their cognitive functions.

NCT ID: NCT02096107 Completed - Graft Dysfunction Clinical Trials

Novartis Everolimus Transition

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

Transition from tacrolimus based triple therapy with Mycophenolate Mofetil (MMF) and steroids in stable renal transplant patients to low intensity tacrolimus, everolimus and prednisone will be associated with improvement in Glomular Filtration Rate (GFR) and allograft fibrosis.