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NCT ID: NCT04322565 Completed - Pneumonia, Viral Clinical Trials

Colchicine Counteracting Inflammation in COVID-19 Pneumonia

ColCOVID-19
Start date: April 20, 2020
Phase: Phase 2
Study type: Interventional

Cytokines and chemokines are thought to play an important role in immunity and immunopathology during virus infections [3]. Patients with severe COVID-19 have higher serum levels of pro-inflammatory cytokines (TNF-α, IL-1 and IL-6) and chemokines (IL-8) compared to individuals with mild disease or healthy controls, similar to patients with SARS or MERS . The change of laboratory parameters, including elevated serum cytokine, chemokine levels, and increased NLR in infected patients are correlated with the severity of the disease and adverse outcome, suggesting a possible role for hyper-inflammatory responses in COVID-19 pathogenesis. Importantly, previous studies showed that viroporin E, a component of SARS-associated coronavirus (SARS-CoV), forms Ca2C-permeable ion channels and activates the NLRP3 inflammasome. In addition, another viroporin 3a was found to induce NLRP3 inflammasome activation . The mechanisms are unclear. Colchicine, an old drug used in auto-inflammatory disorders (i.e., Familiar Mediterranean Fever and Bechet disease) and in gout, counteracts the assembly of the NLRP3 inflammasome, thereby reducing the release of IL-1b and an array of other interleukins, including IL-6, that are formed in response to danger signals. Recently, colchicine has been successfully used in two cases of life-threatening post-transplant capillary leak syndrome. These patients had required mechanically ventilation for weeks and hemodialysis, before receiving colchicine, which abruptly restored normal respiratory function and diuresis over 48 hrs [4].

NCT ID: NCT04322539 Active, not recruiting - Clinical trials for Metastatic Colorectal Cancer

A Study of Efficacy and Safety of Fruquintinib (HMPL-013) in Participants With Metastatic Colorectal Cancer

FRESCO-2
Start date: August 12, 2020
Phase: Phase 3
Study type: Interventional

This is a global, randomized, double-blind, placebo-controlled, multicenter phase 3 clinical trial to compare the efficacy and safety of fruquintinib plus best supportive care (BSC) versus placebo plus BSC in participants with refractory metastatic colorectal cancer (mCRC). 691 participants were randomized to one of the following treatment arms in a 2:1 ratio, fruquintinib plus BSC or placebo plus BSC.

NCT ID: NCT04322513 Recruiting - Coronavirus Clinical Trials

Biomarkers for Identification of COVID-19 Infection

B-DT-COV2
Start date: March 24, 2020
Phase:
Study type: Observational

Acute lung injury represents the most severe form of the viral infection sustained by coronavirus disease 2019 (Covid-19) also named as SARS-CoV-2, a new virus emerged in December 2019 in Wuhan (China). The diagnosis is clinical and patients develop flu-like syndrome with fever and cough; patients with clinical symptoms can perform a swab test, including molecular and/or antigen swab, for diagnosis of positivity to Covid-19. Even if diagnosis and treatment are well described, to date, this viral pandemic infection induces an increased mortality in the world. The aim of the present project is to evaluate specific biomarkers that could be used for patient stratification and for tailor therapy in COVID-19 infected patients.

NCT ID: NCT04322500 Completed - Chalazion Clinical Trials

Probiotics for Chalaziosis Treatment in Children

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

There is growing evidence encouraging the use of probiotics in many conditions in children. The aim of the investigator's study is to define the possible beneficial impact of probiotics on paediatric patients affected by chalaziosis.

NCT ID: NCT04322487 Completed - Coronavirus Clinical Trials

Simple, Safe, Same: Lung Ultrasound for COVID-19

LUSCOVID19
Start date: April 8, 2020
Phase:
Study type: Observational

Growing evidences are showing the usefulness of lung ultrasound in patients with COVID-19. Sars-CoV-2 has now spread in almost every country in the world. In this study, the investigators share their experience and propose a standardized approach in order to optimize the use of lung ultrasound in covid-19 patients. The investigators focus on equipment, procedure, classification and data-sharing.

NCT ID: NCT04322344 Recruiting - Clinical trials for Coronavirus Infections

Escin in Patients With Covid-19 Infection

add-on-COV2
Start date: March 23, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

In December 2019,a new type of pneumonia caused by the coronavirus (COVID-2019) broke out in Wuhan ,China, and spreads quickly to other Chinese cities and 28 countries. More than 70000 people were infected and over 2000 people died all over the world. There is no specific drug treatment for this disease. Considering that lung damage is related to both viral infection and burst of cytokines, our idea is to evaluate the efficacy and safety of escin as add-on treatment to conventional antiviral drugs in COVID-19 infected patients.

NCT ID: NCT04322188 Completed - Clinical trials for Severe Acute Respiratory Syndrome (ARDS) Secondary to SARS-COV-2 Infection

An Observational Study of the Use of Siltuximab (SYLVANT) in Patients Diagnosed With COVID-19 Infection Who Have Developed Serious Respiratory Complications

SISCO
Start date: March 19, 2020
Phase:
Study type: Observational

This observational study will collect data from patients treated with siltuximab program for treatment of SARS-CoV-2 infection complicated with serious respiratory complications. This observational study will group the patients into two cohorts receiving siltuximab.. Outcome of patients will be compared to a cohort of patients receiving standard treatment without siltuximab. The patients will be divided into 2 cohorts. Those contained in Cohort A were treated after the use of continuous positive airways pressure (CPAP) or non-invasive ventilation (NIV). Patients in Cohort B were treated after intubation

NCT ID: NCT04321772 Completed - Exercise Clinical Trials

Muscle Response to High Intensity Interval Resistance Training (HIIRT)

HIIRT
Start date: February 1, 2012
Phase: N/A
Study type: Interventional

Resistance training (RT) is one of the most important stimuli for muscle hypertrophy and it plays an important role on weight loss and fatty acid oxidation increase. RT affects anabolic pathways but the differences among various training techniques has been till now were poorly investigated. The aim of this study was to compare the effect of two different intensity of training, high-intensity interval resistance training (HIIRT) and traditional resistance training (TRT), on muscle signalling pathway.

NCT ID: NCT04321421 Completed - COVID-19 Clinical Trials

Hyperimmune Plasma for Critical Patients With COVID-19

COV19-PLASMA
Start date: March 17, 2020
Phase: N/A
Study type: Interventional

The outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has become pandemic. To date, no specific treatment has been proven to be effective. Promising results were obtained in China using Hyperimmune plasma from patients recovered from the disease.The investigators plan to treat critical Covid-19 patients with hyperimmune plasma.

NCT ID: NCT04320784 Completed - Clinical trials for Fasting and Performance

Effects of a Time Restricted Eating Protocol on Cyclists (TRECYC)

TRECYC
Start date: January 6, 2018
Phase: N/A
Study type: Interventional

We sought to investigate the effects of 4 weeks of 16/8 time restricted eating (TRE) with windows of 16 hours of fasting and 8 hours of eating) on elite cyclists' performance, metabolic and blood parameters.