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Fibrosis clinical trials

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NCT ID: NCT03435939 Recruiting - Cystic Fibrosis Clinical Trials

Effect of Losartan in Cystic Fibrosis (CF)-NIH Grant #133240

Start date: February 15, 2022
Phase: Early Phase 1
Study type: Interventional

The goal of this study is to execute a small clinical proof of concept trial: To examine the effects of losartan on mucociliary clearance (MCC) in patients not eligible for CFTR rescue therapies

NCT ID: NCT03435406 Recruiting - Clinical trials for Hepatopulmonary Syndrome

Investigation of the Prevalence of Hepatopulmonary Syndrome in Cirrhosis Patients Caused by Hepatitis B in Western China

Start date: July 27, 2017
Phase: N/A
Study type: Observational

to investigate the prevalence of hepatopulmonary syndrome in cirrhosis patients caused by Hepatitis B in western China

NCT ID: NCT03433222 Recruiting - Fibrosis Clinical Trials

Phase 1 Study of HF-LED-RL in Fitzpatrick Skin Types I to III

Start date: January 31, 2018
Phase: Phase 1
Study type: Interventional

The goal of this study is to establish the safety of high fluence LED-RL at fluence of 480 J/cm2 and 640 J/cm2 in healthy non-Hispanic, Caucasian subjects. The hypothesis is that high fluence LED-RL phototherapy is safe in non-Hispanic, Caucasians.

NCT ID: NCT03421366 Recruiting - Cystic Fibrosis Clinical Trials

Modified Release Posaconazole in Patients With Cystic Fibrosis

Start date: March 1, 2018
Phase:
Study type: Observational

A prospective single center observational cohort of patients with cystic fibrosis to determine whether adequate serum levels of posaconazole, after administration of the newer modified release once daily oral formulation, can be achieved.

NCT ID: NCT03415698 Recruiting - Cirrhosis, Liver Clinical Trials

G-CSF in Decompensated Cirrhosis: an Open Label Trial

Start date: July 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Globally, cirrhosis is the fifth commonest cause of mortality. Its natural history is typified by an initial, largely asymptomatic, "compensated" phase followed by "decompensation" due to complications of raised portal pressures and hepatocellular dysfunction. Currently the only definitive treatment option for cirrhosis is liver transplantation which is limited in its applicability due to donor shortage, exorbitant costs and lack of widespread availability. The need for long term immunosuppression and its attendant complications are a further drawback. The ability of stem cells to differentiate into multiple cellular lineages makes one speculate that they can be used for tissue repair and regeneration when tissue-resident stem cells become overwhelmed. Bone marrow derived stem cells have amazing plasticity. They can "home" to the liver in response to injury and help in liver regeneration by trans-differentiation, cell fusion and augmentation of tissue- resident stem cell mediated repair. Two methods are available for the mobilisation of stem cells from the bone marrow to the liver. One involves the administration of cytokines like granulocyte-colony stimulating factor (G-CSF) and the other is the isolation of stem cells from the marrow followed by their injection into the hepatic artery or portal vein after purification. The latter is probably more cumbersome and may be potentially risky due to the underlying coagulation abnormalities in cirrhotic patients . G-CSF has been shown to mobilise bone marrow stem cells and even increase survival in patients of severe alcoholic steatohepatitis and ACLF. There is conflicting evidence on the role of G-CSF in decompensated cirrhosis with some studies showing improved survival while others have shown a lack of clinical or biochemical benefit. Many of these studies have used a single course of G-CSF. Verma et al, in a recent study published in 2018, elegantly demonstrated the beneficial effect of multiple courses of G-CSF in improving mortality and transplant free survival in decompensated cirrhotics. The investigators too speculate that multiple cycles of G-CSF could result in better outcomes in decompensated cirrhosis by causing more prolonged and sustained stem cell homing to the liver. Thus, this study is being undertaken to further evaluate the safety and efficacy of multiple cycles of G-CSF in decompensated cirrhotics.

NCT ID: NCT03414398 Recruiting - Liver Cirrhosis Clinical Trials

Assessing Cirrhosis Quality of Care While Accounting for Cost

Start date: December 26, 2017
Phase:
Study type: Observational

The objective of this study is to determine what influences the patient and caregiver perception of care, and if this perception associates with the percentage of and what quality metrics are being met and outcomes. The investigators also plan to capture the cost of providing quality metrics and the cost of monitoring adherence to quality metrics.

NCT ID: NCT03405987 Recruiting - Myocardial Fibrosis Clinical Trials

Association of T1-mapping and LV Strain Analysis by CMR

Start date: July 1, 2012
Phase:
Study type: Observational

The association of T1-mapping (both native and ECV) and strain analysis of LV and RV by CMR will be assessed. Results from strain analysis will be investigated in terms of their prognostic value.

NCT ID: NCT03388151 Recruiting - Cirrhosis, Liver Clinical Trials

Propofol Versus Midazolam for Lower Gastrointestinal Endoscopy

Start date: April 1, 2016
Phase: Phase 3
Study type: Interventional

propofol versus use of midazolam as sedative agent in patients with liver cirrhosis presented for lower gastrointestinal endoscopy

NCT ID: NCT03386890 Recruiting - Liver Fibrosis Clinical Trials

Clinical Application of Non-invasive Assessment for Staging Liver Steatosis and Liver Fibrosis

Start date: December 2015
Phase: N/A
Study type: Observational

Nowadays, the morbidity of Nonalcoholic fatty liver disease (NAFLD) show ascending trend year by year, which has become an important public health problem in China. As NAFLD can progress to Non-alcoholic steatohepatitis (NASH), cirrhosis and Hepatocarcinoma, the identification and quantitative evaluation of liver steatosis and its dynamic changes are crucial. While liver biopsy is still the gold standard in the diagnosis of NAFLD, its application is limited because of the invasive procedure.The Transient Elastography(TE) combined with the Controlled Attenuation Parameter(CAP) is a new non-invasive diagnostic method for fatty liver and liver fibrosis. In order to evaluate the diagnostic value of non-invasive assessment for the degree of liver steatosis and staging liver fibrosis, this non-invasive method will be assessed by the golden standard of liver biopsy among 400 NAFLD patients.The treatment protocols will be decided by doctor and patient both (treatment protocols and medicine are not required). Blood routine, blood biochemistry, abdominal ultrasound and Transient Elastography(TE) combined with the Controlled Attenuation Parameter(CAP) are detected during the follow-up.

NCT ID: NCT03375047 Recruiting - Cystic Fibrosis Clinical Trials

Study to Evaluate the Safety & Tolerability of MRT5005 Administered by Nebulization in Adults With Cystic Fibrosis

RESTORE-CF
Start date: May 10, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This Phase 1/2, first-in-human study will evaluate the safety and tolerability of single and multiple escalating doses of MRT5005 administered by nebulization to the respiratory tract of adult subjects with CF.