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Brain Diseases clinical trials

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NCT ID: NCT05279586 Not yet recruiting - Clinical trials for Hepatic Encephalopathy

Secondary Prophylaxis of Hepatic Encephalopathy in Cirrhotic Patients

Start date: March 2022
Phase: Early Phase 1
Study type: Interventional

The aim of this study is to compare the efficacy and safety of colistin versus lactulose for secondary prophylaxis of overt hepatic encephalopathy in patients with liver cirrhosis.

NCT ID: NCT05239585 Not yet recruiting - Clinical trials for Neonatal Encephalopathy

Remote EEG Device for Identification of Risk for Neonatal Seizures

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to see if the use of wireless brain wave monitoring can be helpful for newborns and help their medical providers identify seizures earlier and to monitor for the risk for seizures.

NCT ID: NCT05229289 Not yet recruiting - Clinical trials for Hepatic Encephalopathy

Efficacy and Safety of Fecal Microbiota Transplant for Secondary Prophylaxis of Hepatic Encephalopathy

Start date: January 31, 2022
Phase: N/A
Study type: Interventional

Despite standard of care, the recurrence of hepatic encephalopathy remains the primary cause for readmissions in individuals with cirrhosis. Patients with cirrhosis have disturbed gut microbiota, which is exacerbated by repeated antibiotic usage. FMT is a promising therapy to restore a healthy microbiota. FMT causes change in composition of gut microbiota which will lead to increase in commensal bacterial diversity which will increase colonization resistance to pathogenic bacteria and thereby decrease the bacterial overgrowth. Healthy bacteria also increase the SCFA production in colon with is and nutrient for endothelial cells and thereby protect the endothelial integrity and decreases bacterial translocation and endotoxemia. Current standard of care mainly focuses on the treatment of precipitating factors of the HE. The goal of our open-label, randomised clinical trial is to evaluate the safety, efficacy of addition of FMT to SOC in preventing subsequent episodes of hepatic encephalopathy.

NCT ID: NCT05140850 Not yet recruiting - Clinical trials for Cognitive Dysfunction

Long-term Consequences of Neuroimaging and Perceived Cognitive Dysfunction in oPRES

Start date: January 2022
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to explore the long-term consequences of neuroimaging and perceived cognitive dysfunction in obstetrics posterior reversible encephalopathy syndrome.

NCT ID: NCT05128305 Not yet recruiting - Cirrhosis, Liver Clinical Trials

Integrated Traditional Chinese and Clinical Medicine for Chronic Hepatitis B and Its Complication

Start date: December 1, 2021
Phase: Phase 3
Study type: Interventional

Hepatic encephalopathy is the most common complication after TIPS, and hepatic encephalopathy occurs in almost all portosystemic shunts. For patients with severe upper gastrointestinal bleeding or refractory ascites in the decompensated chronic hepatitis B, transjugular intrahepatic portosystemic shunt (TIPS) is a very effective treatment. However, due to the severe complications such as hepatic encephalopathy after TIPS, the clinical application of TIPS is limited. Literature studies have shown that the incidence of encephalopathy after TIPS is about 35%. TIPS reduces the portal vena blood flow into the liver by establishing a new channel. But at the same time, the toxic substances from the gastrointestinal tract and other organs do not enter the liver to detoxify, and are more likely to enter the brain, leading to hepatic encephalopathy. Moreover, studies have found that the liver and the intestine originate from the same germ layer and are closely related to each other in anatomy and function. There are a large number of microorganisms living in the intestinal tract. Normally, the intestinal tract, as the first defense of the human body, can effectively prevent bacteria and their products from entering the bloodstream. In cirrhosis and portal hypertension, blood return disorder causes intestinal damage. A series of microbes and product endotoxins such as gram-negative bacteria will enter the blood through the injury, and the toxins in the peripheral blood will enter the brain and cause hepatic encephalopathy happened. The research team's early treatment plan with integrated traditional Chinese and Western medicine proved that it greatly reduced the incidence of hepatic encephalopathy after TIPS. And improve the clinical symptoms and signs of patients with liver cirrhosis, and improve the quality of life and survival of patients.

NCT ID: NCT05065697 Not yet recruiting - Clinical trials for Aortic Valve Stenosis

Brain Lesions After Transcatheter Aortic Valve Replacement

Start date: January 2022
Phase:
Study type: Observational

The Brain lEsions after TrAnscatheter aorTic ValvE Replacement (BETTER) registry is a prospective, observational, multi-center registry aiming to assess the presence of new brain microbleeds assessed on susceptibility-weighted imaging at 3 enrolling sites, in China (West China Hospital, Sichuan University), UK (St Thomas' Hospital) and Denmark (Rigshospitalet, University of Copenhagen). The main study arm is planned to include 100 patients with symptomatic severe aortic stenosis undergoing transfemoral TAVR of any devices and 50 isolated bioprosthetic SAVR patients treated during the enrollment period as a control arm.

NCT ID: NCT04913324 Not yet recruiting - Cerebral Palsy Clinical Trials

Early Virtual Intervention for Infants With CP Following HIE Diagnosis

RECOVER
Start date: June 1, 2021
Phase: N/A
Study type: Interventional

This will be a five year study that will be a prospective, randomized, controlled trial (RCT) to assess the effect of a virtual early intervention care delivery model in the provision of therapy to enhance the neurodevelopmental trajectory of infants with brain injury. In addition, the investigators will enhance understanding of the social and parental contributors to outcomes and the early health economic impact of a virtual clinic. The results of this study will help inform the design of a larger, multi-center randomized controlled trial.

NCT ID: NCT04728438 Not yet recruiting - Sepsis Clinical Trials

Effect of Targeted Temperature Management on Cerebral Autoregulation in Patients With Neurocritical Diseases

Start date: January 22, 2021
Phase:
Study type: Observational

Change and effect of cerebral autoregulation during targeted temperature management in neurocritical patients

NCT ID: NCT04502199 Not yet recruiting - Dysautonomia Clinical Trials

Dysautonomic Phenotype in Male Patients With MECP2 Mutation

MECP2BOYS
Start date: August 15, 2020
Phase:
Study type: Observational

Dysautonomic signs are well known among girls with a Rett Syndrom. Rett syndrom is caused by a MECP2 mutation in 95% of cases. We want to search dysautonomic signs among boys with a MECP2 mutations because they are less studied than the girls and they have more varied phenotypes.

NCT ID: NCT04383808 Not yet recruiting - Brain Disease Clinical Trials

Clinical Translation of a Novel Brain PET Insert for Simultaneous PET/MR

Start date: December 1, 2022
Phase: N/A
Study type: Interventional

The primary goal of this project is to study the feasibility of a brain-dedicated PET insert for an MR scanner for simultaneous acquisition of PET/MR images of human brains. The study will also allow us to compare the imaging performance of the investigator's brain-dedicated PET insert against a commercial whole-body permanently integrated PET/MRI system using a common radiopharmaceutical.