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Hypoxia clinical trials

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NCT ID: NCT01481207 Completed - Clinical trials for Hypoxic Ischemic Encephalopathy

Magnetic Resonance Imaging and Spectroscopy Biomarkers of Neonatal Hypoxic Ischemic Encephalopathy

Start date: September 2011
Phase:
Study type: Observational

Neonatal hypoxic ischemic encephalopathy (HIE) is a serious neurological condition characterised by acute or subacute brain injury arising from perinatal hypoxia. HIE is thought to affect approximately 0.2% of live births, and is associated with a high risk of mortality or long-term neurological disability. Accurate biomarkers for long-term neuro-developmental outcome following HIE are extremely important both for clinical management and the evaluation of therapeutic approaches. According to a recent meta-analysis, the ratio of the cerebral concentrations of lactate and N-acetyl aspartate (NAA), two neuro-metabolites detectable with magnetic resonance spectroscopy (MRS), currently represents the most accurate prognostic indicator of outcome following HIE. However, for various technical reasons standard MRS methods do not offer optimal sensitivity for detecting lactate, which may potentially be improved with a custom lactate editing MRS sequence. In addition, while perfusion has also been suggested as a potential biomarker for neuro-developmental outcome following HIE, due to a paucity of MR perfusion imaging studies in neonates, the prognostic accuracy of perfusion MR measures has not been evaluated in comparison with more established MR biomarkers. The aims of this study are: 1. to evaluate the relative sensitivity of a custom lactate editing MRS pulse sequence (specialist software) relative to the standard point resolved (PRESS) MRS sequence for detecting lactate in neonates with suspected HIE. 2. to evaluate the sensitivity and specificity of MR perfusion measures in comparison to MRS measures as predictors of neuro-developmental outcome at 2 years.

NCT ID: NCT01464216 Active, not recruiting - Prostatic Neoplasms Clinical Trials

MRI for Assessment of Hypoxia-Induced Prostate Cancer Aggressiveness

FuncProst
Start date: October 2011
Phase:
Study type: Observational

The purpose of the study is to combine and correlate data from morphological and functional MRI, molecular signatures of tumor hypoxia, the presence of micrometastases and tumor hypoxia with the goal being predicting of prostate cancer aggressiveness.

NCT ID: NCT01463527 Completed - Hypoxia Clinical Trials

Using Capnography to Reduce Hypoxia During Pediatric Sedation

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

The investigators hypothesize that the addition of capnography during moderate sedation will improve recognition of hypoventilation and apnea. This will lead to an increased frequency of staff interventions such as verbal or physical stimulation for these events in order to improve ventilation which will in turn lead to a reduction in the frequency of oxygen desaturations. If capnography proves to be effective in creating earlier detection and intervention for hypoventilation and apnea during moderate sedation provided by non-anesthesiologists, this device can be used in a variety of clinical settings to enhance patient safety.

NCT ID: NCT01408329 Completed - Hypoxia Clinical Trials

Effects of Cyclic Variations in Altitude Conditioning (CVAC) on Wellness and Activity Measures

CVAC
Start date: January 2007
Phase: N/A
Study type: Interventional

Cyclic Variation in Altitude Conditioning (CVAC) is a new technique that uses a pod-like device to expose users to controlled fluctuations in air pressure. It is designed to promote quicker altitude acclimatization, thus promoting improvements in exercise capacity at altitude and, possibly, at sea level. However, over the past few years, anecdotal stories from users of the device suggest that the CVAC treatments might be causing changes beyond the expected endurance exercise performance benefits. Therefore, the purpose of the study is to obtain data on some of the previous anecdotal claims regarding the device (e.g. increases in strength, improved glucose tolerance, reduction of neuropathic pain and decreased joint swelling) as well as to obtain broad questionnaire data in order to identify more specific variables to investigate in future studies.

NCT ID: NCT01386814 Not yet recruiting - Hypoxia Clinical Trials

Neuropsychological Sleep Physical Exercise Hypoxia

Hypoxia
Start date: July 2011
Phase: N/A
Study type: Observational

Aim: To evaluate the influence of oxygen deficit on the cognitive performance and also about the architecture and sleep efficiency in volunteers subjected to mild and moderate exercise in a hypobaric chamber. SUMMARY: Participants in this study 30 healthy male volunteers, aged 20 to 40 years, regular physical activity, constituting three groups: 1 - without exercise-hypoxia group 10 volunteers who not be subjected to any kind of physical exercise in hypoxia and remain all day of experiment, 2 - group exercise at sea level, is composed of 10 volunteers who will undergo a protocol exercise physical sea-level, 3 - group exercise and hypoxia - 10 volunteers who will carry out a protocol exercise on a treadmill, being the same in condition of hypoxia (hypobaric chamber). All groups on the first day of the experiment will undergo baseline assessments, laboratory blood analysis salivary and spirometric testing. Assessments will be personality and neuropsychological. After baseline assessments, the last day of the experiment, the groups will be evaluated again 4350m above sea level the sea, by personality tests, neuropsychological and laboratory. RATIONALE AND BACKGROUND: During exposure to environments with a partial reduction of oxygen, human body can undergo several physiological and psychological changes are not prepared for such condition. Few studies have reported that the elevation changes and cognitive aspects related to sleep. MATERIAL AND METHOD: They describe the procedures to be performed, and the study conducted in local with adequate infrastructure.

NCT ID: NCT01317329 Completed - Obesity Clinical Trials

"Reversibility of Cardiovascular Injury With CPAP Use: Mechanisms Involved"

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

The purpose of this study is to determine the factors that are associated with improved cardiovascular function with the use of CPAP therapy on subjects diagnosed with moderate to severe obstructive sleep apnea.

NCT ID: NCT01279746 Completed - Hypoxia Clinical Trials

The Diagnosis of Occult Deep Vein Thrombosis of the Lower Extremities in Patients Presenting With Hypoxia

Start date: April 2010
Phase: N/A
Study type: Observational

The purpose of this study is to prove that bedside Ultrasound Compression is a useful screening tool for the diagnosis of occult deep vein thrombosis in patients presenting to the emergency room with hypoxia.

NCT ID: NCT01260428 Recruiting - Hypoxia Clinical Trials

Effects of Expiratory Pressure on Arterial Oxygenation During Hypoxia

hypex
Start date: February 2011
Phase: N/A
Study type: Observational

Altitude tolerance correlates with the level of oxygenation achieved. The aim of the present study is to investigate whether increased expiratory pressure within the thorax is able to improve oxygenation during hypoxic hypoxia.

NCT ID: NCT01253785 Completed - Hypoxia Clinical Trials

Pulse Oximeter Responses to Multiple Levels of Stable Hypoxia

Start date: May 2010
Phase: N/A
Study type: Observational

Validate pulse oximeter sensor SpO2 accuracy from 70-100% during induced hypoxia.

NCT ID: NCT01253772 Completed - Hypoxia Clinical Trials

Pulse Oximeter Responses to Multiple Levels of Stable Hypoxia in Neonates

Start date: May 2010
Phase: N/A
Study type: Observational

Validate pulse oximeter sensors in neonates by comparing sensor readings to blood samples during cardiac surgery.