Clinical Trials Logo

Fibrosis clinical trials

View clinical trials related to Fibrosis.

Filter by:

NCT ID: NCT02039986 Completed - Cystic Fibrosis Clinical Trials

Ivacaftor (Kalydeco) and Insulin in Cystic Fibrosis (CF)

Start date: January 6, 2014
Phase:
Study type: Observational

This study is aimed at better understanding the impact of ivacaftor upon insulin and incretin secretion and glucose tolerance in patients with Cystic Fibrosis with a glycine (G551D) mutation. Investigators hypothesize that treatment with ivacaftor improves insulin secretion in individuals with CF.

NCT ID: NCT02038803 Completed - Cystic Fibrosis Clinical Trials

Efficacy of TOBI Podhaler vs. Tobramycin Inhalation Solution

PETIS
Start date: October 2013
Phase:
Study type: Observational

Inhaled tobramycin is a Cystic Fibrosis Foundation recommended effective treatment for individuals with cystic fibrosis for the management of Pseudomonas aeruginosa airway colonization and improves the FEV1 and reduces the number of acute pulmonary exacerbations of CF. Patients typically use the inhaled tobramycin for a period of 28 days. Unfortunately, the standard nebulizer method for delivering tobramycin inhaled solution (TIS) is time-consuming and may result in missed therapy doses and suboptimal care. A new inhaled formulation and delivery device, the TOBI Podhaler (TPI), is a quicker, more efficient method of administering inhaled Tobramycin. This new pocket-sized disposable inhaler is maintenance free, requires no refrigeration or power source, and should greatly increase patient mobility and improve time management.

NCT ID: NCT02036970 Completed - Clinical trials for Pulmonary Hypertension

Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT

Start date: May 31, 2014
Phase: Phase 2
Study type: Interventional

This study assesses the safety and efficacy of bardoxolone methyl relative to placebo in patients with pulmonary hypertension to determine the recommended dose range, evaluate the change from baseline in 6-minute walk distance (6MWD) and determine the effect of Bardoxolone methyl in pulmonary hypertension associated with connective tissue disease, interstitial lung disease, and idiopathic etiologies, including subsets of patients with WHO Group III or WHO Group V PH following 16 weeks of study participation.

NCT ID: NCT02036879 Completed - Clinical trials for Cystic Fibrosis (CF)

Gender Disparity and Hormones in Cystic Fibrosis

Start date: February 2014
Phase: Early Phase 1
Study type: Interventional

The objective of this study is to investigate the impact of hormones on lung disease in Cystic Fibrosis (CF) patients. Due to improved therapies, CF patients are living longer and healthier lives than they did 20 years ago. However, females have been shown to have a survival disadvantage. The median life expectancy is 33 in women and 37 in men with CF. The hypothesis is that estrogen and/or progesterone negatively impact lung health in CF. Therefore, understanding the impact of sex hormones (including the use of birth control pills) on the disease process is increasingly important. The purpose of this study is to determine if lung function, respiratory symptoms, or various markers of lung health change during different phases of the natural ovulatory cycle in order to understand if estrogen or progesterone hormones are impacting the disease relative to fluctuations in men with stable testosterone levels. The research objectives of this project are to: - Determine if lung function, respiratory symptoms, or various markers of lung health change during different hormonal phases of the ovulatory cycle in women. - Determine if men change lung function, respiratory symptoms, or various markers of lung health over time. - Determine if oral contraceptive pills in women stabilize fluctuations in symptoms and improve lung health.

NCT ID: NCT02036580 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

D2212C00002 J-Phase II Study

Start date: January 2014
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the safety and tolerability of multiple-doses of tralokinumab in Japanese patients with Idiopathic Pulmonary Fibrosis.

NCT ID: NCT02031913 Completed - Chronic Hepatitis B Clinical Trials

Prospective Cohort Study of Association of Insulin Resistance/Steatosis With Hepatic Fibrosis in CHB and NAFLD

Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

Hepatic steatosis and insulin resistance are associated with severity of fibrosis in non-alcoholic fatty liver disease (NAFLD) and chronic hepatitis C. However, clinical significance of steatosis and insulin resistance on fibrosis in chronic hepatitis B (CHB) is not well established. The aim was to investigate the relationship between insulin resistance, hepatic steatosis, and fibrosis in patients with CHB.

NCT ID: NCT02029521 Completed - Cystic Fibrosis Clinical Trials

Supplementation of Oral Reduced Glutathione in Pediatric Cystic Fibrosis Patients

Start date: March 2011
Phase: N/A
Study type: Interventional

Many individuals with cystic fibrosis experience growth failure. The reasons are not clear, but inflammation of the gut in these patients seems to be one important reason. Glutathione is important to normal function of the intestine and lungs. Glutathione functions to decrease inflammation and to thin mucus. However, in cystic fibrosis, glutathione gets trapped inside of cells, so it cannot travel to the surface of the cells and perform its proper function. Moreover, glutathione has been shown to improve nutritional status in patients with AIDS and cancer. Investigators hypothesize that supplementation of oral glutathione to pediatric individuals with cystic fibrosis could improve growth failure.

NCT ID: NCT02028949 Completed - Clinical trials for Unresectable Non-metastatic Hepatocellular Carcinoma

Treatment of Cirrhosis-related Hepatocellular Carcinoma With the Intrahepatic Arterial Injection of an Emulsion of Lipiodol and Idarubicin (Zavedos®): Phase I Study

Start date: November 22, 2012
Phase: Phase 1
Study type: Interventional

Unresectable, non-metastatic cirrhosis-related hepatocellular carcinoma (HCC) has a poor prognosis as there are no recommended curative treatments. Chemoembolisation is the most widely used treatment in these patients, but this technique can prove to be toxic. intrahepatic arterial chemotherapy with lipiodol and idarubicin could be an effective therapeutic approach, without deteriorating liver function. The rationale for this treatment can be resumed as follows: - HCC are vascularised via the hepatic artery system - The IHA perfusion of anthracyclines leads to high elimination via the liver with low systemic concentrations - The absence of embolisation reduces toxicity - the toxiciity profile of idarubicin is well known and the drug is widely used for the IV treatment of leukemia - idarubicin is the most cytotoxic drug for tumor cell lines. - The in vitro cytotoxicity of idarubicin is 100% at low concentrations - Lipiodol can stay in contact with tumor tissue for several weeks after injection and act as a vector for the drug - The idarubicin-lipiodol is more stable than lipidol emulsions usually given by intraarterial injection - The emulsion is more stable with idarubicin than with other anticancer molecules - Sequential inclusion in accordance with the "continual reassessment method" makes it possible to increase inclusions at a target toxicity level while reducing inclusions at doses that are too low or too toxic The aim of the treatment is to improve survival.

NCT ID: NCT02026401 Completed - Clinical trials for Primary Biliary Cirrhosis

Phase 2 Study of NGM282 in Patients With Primary Biliary Cirrhosis

Start date: February 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, and activity of NGM282 in patients with Primary Biliary Cirrhosis.

NCT ID: NCT02025829 Completed - Cystic Fibrosis Clinical Trials

IL-17 Neutrophils in CF Lung Inflammation

Start date: February 2014
Phase:
Study type: Observational

The purpose of this study is to determine whether IL-17 polymorphonuclear leukocytes (PMNs) are central to the disease pathology in CF. This will be determined by demonstrating that IL-17 PMNs are present in the CF airway, correlate with lung function measures, and decrease in patients being treated with IV antibiotics for a pulmonary exacerbation.