Clinical Trials Logo

Fibrosis clinical trials

View clinical trials related to Fibrosis.

Filter by:

NCT ID: NCT02778425 Completed - Portal Hypertension Clinical Trials

The Treatment of Hepatocirrhosis and Portal Hypertension

Start date: February 2016
Phase: N/A
Study type: Interventional

This study compare the efficiency of partial splenic embolization +endoscopical therapy with endoscopical therapy alone in gastroesophageal variceal haemorrhage accompanied with splenomegaly or hypersplenism of hepatocirrhosis and portal hypertension treatment.

NCT ID: NCT02776098 Completed - Cystic Fibrosis Clinical Trials

Muscle Accrual and Function in Cystic Fibrosis-Impact of Glucose Intolerance

Start date: May 2016
Phase:
Study type: Observational

This study will investigate the link between glucose abnormalities and elements critical to muscle function including mass, composition and energy metabolism. the primary goal of the study is to determine whether Cystic Fibrosis (CF) disease is associated with muscle dysfunction, especially in the presence of glucose intolerance. This is a longitudinal cohort study of 3 main groups: CF subjects without Cystic Fibrosis-related diabetes (CFRD), healthy matched controls and CF subjects with newly diagnosed CFRD started on insulin therapy.

NCT ID: NCT02774161 Completed - Cirrhosis Clinical Trials

B-mode Ultrasound Imaging in Detecting Early Liver Cancer

Start date: May 2016
Phase: N/A
Study type: Interventional

This pilot trial studies how well B-mode ultrasound imaging works in detecting liver cancer that is early in its growth and may not have spread to other parts of the body. Diagnostic procedures, such as B-mode ultrasound imaging, may help find and diagnose liver cancer and find out how far the disease has spread.

NCT ID: NCT02767297 Completed - Cystic Fibrosis Clinical Trials

Bioavailability and Pharmacokinetics Study of FDL169 in Healthy Subjects and Subjects With Cystic Fibrosis

Start date: April 2016
Phase: Phase 1/Phase 2
Study type: Interventional

To determine the relative bioavailability of the capsule (reference) and tablet (test) formulations of FDL169 in healthy adult males and females, and to evaluate the pharmacokinetic (PK) profile FDL169 tablets (test formulation) in both healthy adult males and females, and subjects with cystic fibrosis (CF).

NCT ID: NCT02758808 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis (IPF)

Pulmonary Fibrosis Foundation Patient Registry

PFFR
Start date: March 29, 2016
Phase:
Study type: Observational [Patient Registry]

The Pulmonary Fibrosis Foundation Patient Registry will collect data on at least 2,000 patients with interstitial lung disease (ILD) at approximately 40 clinical sites in the US. The Registry is targeting enrollment of approximately 60% of the 2,000 ILD participants to have idiopathic pulmonary fibrosis (IPF). The aim of the Registry is to create a cohort of well-characterized patients with interstitial lung disease (ILD) for participation in retrospective and prospective research

NCT ID: NCT02750722 Completed - Cystic Fibrosis Clinical Trials

Exercise and Oscillatory Positive Expiratory Pressure Therapy in Cystic Fibrosis

Start date: May 2016
Phase: N/A
Study type: Interventional

The investigators aim to compare a single bout of moderately intense cycling exercise incorporating Flutter® breathing maneuvers with a single bout of moderately intense cycling exercise alone on sputum viscoelasticity (primary endpoint) and the diffusion capacity of the lungs in adult patients with cystic fibrosis. The investigators further aim to analyze the short-term variability of resting diffusion capacity of carbon monoxide (DLCO) and nitric oxide (DLNO) in patients with cystic fibrosis.

NCT ID: NCT02750501 Completed - Cystic Fibrosis Clinical Trials

Absorption and Safety With Sustained Use of RELiZORB Evaluation (ASSURE) Study

ASSURE
Start date: July 20, 2016
Phase: N/A
Study type: Interventional

Protocol 0000498: Multicenter, open label study to evaluate the effect of sustained RELiZORB (immobilized lipase) cartridge use during enteral feeding on fat absorption, as well as safety and tolerability of sustained RELiZORB use, in patients with cystic fibrosis and exocrine pancreatic insufficiency.

NCT ID: NCT02745184 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Clinical Efficacy and Safety of Autologous Lung Stem Cell Transplantation in Patients With Idiopathic Pulmonary Fibrosis

Start date: March 30, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

Idiopathic pulmonary fibrosis (IPF) is a chronic and ultimately fatal disease characterized by a progressive damage of lung structure and decline in lung function.This study intends to carry out an open, single-center, non-randomized, self control phase I clinical trial. During the treatment, lung stem cells will be isolated from patients' own bronchi and expanded in vitro. Cultured cells will be injected directly into the lesion by fiberoptic bronchoscopy after lavage. After 24-week observation, the investigators will evaluate the safety and efficacy of the treatment by measuring the key clinical indicators.

NCT ID: NCT02739217 Completed - Diabetes Clinical Trials

Safety and Tolerability of PBI-4050 and Its Effects on the Biomarkers in Subjects With Alström Syndrome

Start date: February 22, 2016
Phase: Phase 2
Study type: Interventional

This is a Phase 2, single-centre, single-arm, open-label study of the safety, tolerability, and effects on biomarkers of PBI-4050 in subjects with Alström syndrome for a treatment duration of 24 weeks. Subjects who complete the initial 24 weeks of treatment may continue treatment for an additional 36 or 48 weeks, provided the subject signs informed consent.

NCT ID: NCT02739165 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Clinical Study of ART-123 for the Treatment of Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Start date: May 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of the intravenous drip infusion of ART-123 in patients with acute exacerbation of idiopathic pulmonary fibrosis (IPF) in a multicenter, double-blind, randomized, placebo-controlled, parallel group comparison study, and to confirm its superiority over placebo with survival rate on Day 90 as the primary endpoint.