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Fibrosis clinical trials

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NCT ID: NCT01784419 Completed - Cystic Fibrosis Clinical Trials

Short Term Effects of Ivacaftor in Non-G551D Cystic Fibrosis Patients

Start date: October 2013
Phase: N/A
Study type: Interventional

This is a study of the short-term effects of ivacaftor on sweat chloride concentration and lung function in cystic fibrosis (CF) patients who fall outside current FDA approval. This new, first of its kind drug is approved for use only in CF patients with the G551D mutation in whom it safely confers considerable benefits. However, it is highly likely that CF patients with many other mutations can benefit similarly from this drug, some of whom can be identified by phenotype or genotype. We will enroll up to 30 CF subjects with clinical presentations in which there is one or more signs of residual CF channel function. The signs of residual function include: normal digestion, concentration of chloride in sweat between 55 and 85, or milder than expected CF disease in a CF patient with severe gene mutations. The primary outcome measure will be the difference in sweat chloride concentration measured in subjects on placebo and on ivacaftor. Secondary outcome measured will be lung function.

NCT ID: NCT01783613 Completed - Cystic Fibrosis Clinical Trials

Eficacy of Long-term Suplementation With Docosahexaenoic Acid in Patients With Cystic Fibrosis

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

Cystic Fibrosis (CF) is a congenital disease secondary to the abnormal function of CFTR. Patients with CF have an alteration of essential fatty acids, Arachidonic Acid (AA) is increased and Docosahexanoic Acid (DHA) is decrease and the ratio ω-6/ ω-3 is elevated, all these alterations stimulated a chronic and bad regulated state of inflammation. For this porpoise, a fase IV trial, multicentric, controlled, double blind, placebo and parallel in patients elder than two months old and randomized to received every day a dietetically supplement with DHA or placebo, will be done during 12 months. The trial has as a principal objective to proved if this long term supplementation could decrease in contrast with placebo.

NCT ID: NCT01781832 Completed - Bladder Fibrosis Clinical Trials

Bladder ARFI (Acoustic Radiation Force Impulse) Study

Start date: October 2012
Phase: N/A
Study type: Interventional

Urinary bladder fibrosis (thickening and scarring) is fairly uncommon in children. Traditionally, the presence of urinary bladder fibrosis has been confirmed directly with bladder biopsy or using urodynamic testing. In this study we will use ultrasound scanning and ARFI (acoustic radiation force impulse) wave velocities to potentially identify any urinary bladder wall fibrosis.

NCT ID: NCT01777373 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Conducting Airways in Lung Fibrosis (VACFI)

VACFI
Start date: August 2012
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether extension of the conducting airways into the distal lung, or bronchiolization, occurs early in the course of Idiopathic Pulmonary Fibrosis, a disease wherein normal lung structures are destroyed and replaced by non-functional scar tissue.

NCT ID: NCT01772758 Completed - Cystic Fibrosis Clinical Trials

Cystic Fibrosis and Endothelial Function: At Rest and During Exercise

Start date: August 2011
Phase: Phase 2
Study type: Interventional

Perhaps one of the most disturbing aspects of Cystic Fibrosis (CF) is the associated premature death. Oxidative stress has been observed in patients with CF and exercise intolerance has been shown to predict mortality in patients with CF, regardless of how healthy their lungs are. A critical barrier to improving the quality of life and longevity in patients with CF is our lack of knowledge regarding the different reasons why patients with CF cannot exercise to the level of their peers. We have collected preliminary data to support our central hypothesis that oxidative stress contributes to the impairment in blood vessel function at rest and during exercise which ultimately oxygen transport and delivery resulting in exercise intolerance. Exercise is therapeutic medicine for patients with CF and this investigation represents a major breakthrough in the approach to begin understanding the physiological mechanisms which contribute to exercise intolerance in these patients.

NCT ID: NCT01772667 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Long Term Effects of an Inpatient Pulmonary Rehabilitation Program in Patients With Pulmonary Fibrosis

Start date: October 2013
Phase: N/A
Study type: Interventional

There is evidence that an inpatient pulmonary rehabilitation of 3 weeks improves exercise capacity and quality of life in patients with idiopathic pulmonary fibrosis. However, there are no data available regarding long-term effects of this multimodal program. The aim of this study is to investigate the long-term impact of a rehabilitation program 3 month after finishing on exercise capacity and physical activity.

NCT ID: NCT01771991 Completed - Clinical trials for Radiation Induced Fibrosis to the Head and Neck

Study of Topical Superoxide Dismutase to Treat Radiation Induced Fibrosis

Sodermix
Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if topical superoxide dismutase is an effective treatment of radiation related neck fibrosis, and to determine the quality of life impact from radiation related fibrosis in the head and neck cancer patients at Sanford Health.

NCT ID: NCT01766817 Completed - Clinical trials for Idiopathic Pulmonary Fibrosis

Safety and Efficacy of a Lysophosphatidic Acid Receptor Antagonist in Idiopathic Pulmonary Fibrosis

Start date: January 31, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if study drug (BMS-986020) dose of 600 mg once daily or 600 mg twice daily for 26 weeks compared with placebo will reduce the decline in forced vital capacity (FVC) and will be well tolerated in subjects with idiopathic pulmonary fibrosis (IPF).

NCT ID: NCT01759342 Completed - Cystic Fibrosis Clinical Trials

Comprehensive Exercise Training Program During Hospitalization for an Acute CF Exacerbation

Start date: April 2008
Phase: N/A
Study type: Interventional

This protocol was designed to assess if when subjects with CF are admitted to the hospital for a pulmonary exacerbation if a comprehensive exercise program (moderate to high intensity aerobic, resistance, flexibility and balance exercises) was superior to our "usual care intervention (30 min/day of self selected mode and intensity of exercise) in improving aerobic capacity, muscle strength/power, flexibility and balance.

NCT ID: NCT01756794 Completed - Alcoholic Hepatitis Clinical Trials

Validation of the Procedure of Early Liver Transplantation in Alcoholic Hepatitis Resisting to Medical Treatment

QuickTrans
Start date: December 5, 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to validate a strategy of identification of patients for early liver transplantation in severe alcoholic hepatitis. In this setting, short-term survival is very low (approx. 25% at 6 months) and a pilot study has suggested (mathurin et al. N Engl J Med 2011) that liver transplantation may be an option in very carefully selected patients who did not respond to medical treatment. This selection process deserves to be confirmed in a population of greater size. We hypothesized that patients selected with this process would have a same alcohol relapse rate after liver transplantation than patients transplanted for alcoholic cirrhosis and selected using a 6-month sobriety period