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Brain Diseases clinical trials

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NCT ID: NCT02544542 Completed - Clinical trials for Hypoxic-Ischemic Encephalopathy

Clinical Trial of a New Rectum Cooling System on Patients of Hypoxic-ischemic Brain Damage

Start date: January 2014
Phase: N/A
Study type: Interventional

This study will try to evaluate the effectiveness and safety of a new method for achieving mild hypothermia, i.e.,mild hypothermia therapy through rectum. Half of participants will be treated by the widely-used hyper-hypothermia blanket method, while the other half will be treated by the investigators' new method.

NCT ID: NCT02544100 Recruiting - Clinical trials for Neonatal Encephalopathy

Neonatal Neurologic Intensive Care Network of China

Start date: September 1, 2015
Phase:
Study type: Observational

The purpose of this study is to create a neonatal neurologic biological big data center named Neonatal Neurologic Intensive Care Network in China with neonatal systematic information, biological samples and genomics & genetic data on neonates born with neonatal severe encephalopathy. It also can predict brain injury as cerebral function monitoring through big data and recommend appropriate treatment. In addition, the following samples will be collected in a bio-bank in for future studies: blood, urine, and cerebrospinal fluid (CSF) samples.

NCT ID: NCT02529202 Completed - Clinical trials for Hypoxic-ischemic Encephalopathy

Dexmedetomidine Pharmacokinetics in Neonates During Therapeutic Hypothermia

Start date: March 2016
Phase: Phase 0
Study type: Interventional

The goal of this proposal is to profile the pharmacokinetics of dexmedetomidine in newborns ≥36 weeks post-menstrual age during therapeutic hypothermia for hypoxic-ischemic encephalopathy.

NCT ID: NCT02520817 Completed - Clinical trials for Minimal Hepatic Encephalopathy

Antioxidants and Zinc Improving Minimal Hepatic Encephalopathy In Truck Drivers; a Pilot Study

Start date: January 2013
Phase: N/A
Study type: Observational

Minimal hepatic encephalopathy (MHE) can have a far-reaching impact on quality and ability to function in daily life and may progress to overt Hepatic Encephalopathy. Patients with MHE were missed in clinical follow up and are more exposure to work accident. The aim of the present study was to assess the effects of oral supplementation of antioxidant and zinc gluconate Versus Lactulose inTruck driver cirrhotic patients with MHE.

NCT ID: NCT02488993 Completed - Clinical trials for Hepatic Encephalopathy

Real World Outcomes Study of Hepatic Encephalopathy Patients' Experience on Rifaximin (PROSPER)

PROSPER
Start date: June 2015
Phase:
Study type: Observational [Patient Registry]

This study evaluates hepatic encephalopathy (HE) and liver-related hospitalization rates and duration of stay in patients with HE treated with rifaximin-α 550mg compared to patients receiving other therapies. This registry study aims to comprehensively and rigorously characterize the impact of rifaximin-α 550 mg on hospitalization, clinical safety and effectiveness outcomes, and quality of life in patients with HE in Europe and Australasia.

NCT ID: NCT02470546 Recruiting - Liver Cirrhosis Clinical Trials

Metformin Experience on Minimal Hepatic Encephalopathy

EME
Start date: March 2015
Phase: Phase 4
Study type: Interventional

Primary aim: -To assess the effect of metformin use on the treatment of minimal hepatic encephalopathy in patients with liver cirrhosis. Secondary aim: -To evaluate if metformin is a safety drug in patients showing liver cirrhosis.

NCT ID: NCT02464124 Recruiting - Clinical trials for Encephalopathy, Hepatic

Nitazoxanide Plus Lactulose Versus Lactulose Alone Treatment of Hepatic Encephalopathy

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

Hepatic encephalopathy (HE) is a reversible neuropsychiatric syndrome associated with chronic and acute liver dysfunction. It is characterized by cognitive and motor deficits of varying severity. Treatment options include lactulose administered orally or by nasogastric tube or enema, non-absorbable antibiotics, and protein-restricted diets. Nitazoxanide is an oral agent indicated for the treatment of infectious diarrhea caused by Crytpsporidiumparvum and Giardia lamblia. Basu and colleagues presented a pilot prospective study at the 2008 American Association for the Study of Liver Diseases meeting showing clinical improvement in HE among cirrhotic patients who received nitazoxanide and lactulose.

NCT ID: NCT02455830 Active, not recruiting - Clinical trials for Neonatal Encephalopathy (Neonatal Hypoxic-ischemic Encephalopathy)

Cytokines Associated With Cord Blood Cell Therapy for Neonatal Encephalopathy

Start date: April 2015
Phase:
Study type: Observational

This is a observational study to assess the effects of and to explore the mechanisms of autologous umbilical cord blood cell therapy for neonatal encephalopathy by way of measuring serum cytokines.

NCT ID: NCT02451618 Terminated - Seizures Clinical Trials

Novel Epidermal Recording and Detection of Seizures

NERDS
Start date: January 27, 2015
Phase:
Study type: Observational

For any newborn that exhibits possible seizure activity or has altered mental status of unknown etiology, continuous bedside EEG recording is the standard of care to detect subclinical seizure activity. The experimental aspect of this study will be the application of test electrodes (EES or EKG) to evaluate if the electrodes can be used to produce a continuous bedside recording of brain activity in the same manner as an EEG recording, while ideally producing less irritation of newborn skin than conventional EEG electrodes.

NCT ID: NCT02445417 Completed - Encephalopathy Clinical Trials

Brain Activity During Birth for Prediction of Newborns at Risk for Brain Injury

Start date: June 25, 2015
Phase:
Study type: Observational

The purpose of this study is early identification of asphyxiated newborns through eeg starting in the delivery room.