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Hypoxia clinical trials

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NCT ID: NCT00902577 Completed - Adult Glioblastoma Clinical Trials

MRI and PET/FMISO In Assessing Tumor Hypoxia in Patients With Newly Diagnosed Glioblastoma Multiforme

Start date: August 24, 2009
Phase: Phase 2
Study type: Interventional

This phase II trial is studying how well positron emission tomography (PET) scan using 18F-fluoromisonidazole works when given together with magnetic resonance imaging (MRI) ) in assessing tumor hypoxia in patients with newly diagnosed glioblastoma multiforme (GBM). Diagnostic procedures, such as MRI and PET scan using 18F-fluoromisonidazole (FMISO), may help predict the response of the tumor to the treatment and allow doctors to plan better treatment.

NCT ID: NCT00860743 Completed - Clinical trials for Sleep Apnea Syndromes

Respiratory and Autonomic Plasticity Following Intermittent Hypoxia

RAP-IH
Start date: September 2009
Phase: Early Phase 1
Study type: Interventional

The prevalence of obstructive sleep apnea is high in the Veteran population. If not treated promptly, sleep apnea may result in daytime fatigue which may lead to increased prevalence of accidents while driving or in the workplace. Recent large scale epidemiological studies have shown that the prevalence of excessive daytime sleepiness increases in individuals who suffer from obstructive sleep apnea. Obstructive sleep apnea may also result in the development of hypertension and other cardiovascular disorders. Previous findings have shown that subjects with sleep apnea have a greater risk for developing coronary vascular disease compared to individuals that do not suffer from sleep apnea Thus, a significant amount of evidence suggests that sleep apnea is a major health concern in the Veteran population. Consequently, determining the mechanisms that may impact on the severity of sleep apnea and increase the prevalence of cardiovascular incidents associated with this disorder is important, as is discovering novel treatments.

NCT ID: NCT00859950 Completed - Clinical trials for Obstructive Sleep Apnea

Mechanisms of Endothelial Cell Dysfunction in Sleep Apnea

Start date: April 2009
Phase: N/A
Study type: Interventional

Sleep apnea is a common sleep disorder characterized by temporary stops in breathing during sleep and has been associated with the development of cardiovascular disease. This research will investigate one potential mechanism leading to the development of cardiovascular disorder, specifically, the blockage of blood vessels called "vascular occlusion", in subjects with sleep apnea. A group of healthy controls will be used for comparison. All subjects will undergo clinical evaluation followed by an overnight sleep study and a morning blood draw. Subjects with sleep apnea will be treated according to standard clinical management and followed under the research protocol for one month. At the end of one month, a repeat blood draw will be performed on the sleep apnea subjects for comparative analysis. If a control subject is found to have any abnormality during this research study, he or she will be referred for further clinical evaluation.

NCT ID: NCT00830453 Completed - Stroke Clinical Trials

Hyperbaric Oxygen Therapy in Chronic Stable Brain Injury

HYBOBI
Start date: November 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to discover the feasibility of conducting clinical research in individuals with chronic sequelae following brain injury who are given hyperbaric oxygen. This study will also look at the outcome of individuals with a chronic stable brain injury due to trauma, anoxia (lack of oxygen to the brain), or stroke, who are given hyperbaric oxygen. Outcome measures testing cognitive (memory, etc.) and functional (balance, strength, etc.) measures will be performed before the hyperbaric sessions, immediately following them, and 6 months later. The subject will receive 60 hyperbaric sessions, 60 minutes in the chamber, to a pressure of 1.5 ATA, once daily, Monday through Friday.

NCT ID: NCT00788983 Completed - Hypoxia Clinical Trials

Induced Hypoxia Study for Validation of SpO2 Accuracy

Start date: November 2008
Phase: N/A
Study type: Observational

Validate Non-Motion SpO2 Accuracy from 70%-100% of various pulse oximeter/ sensor combinations and various OEM pulse oximeter modules and sensor combinations during induced hypoxia (desaturation).

NCT ID: NCT00782977 Completed - Hypoxia Clinical Trials

Apneic Oxygenation Via Nasal Cannulae Prevents Arterial Hypoxemia

Start date: November 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the effectiveness of continuous oxygen provided by nasal prongs in preventing or delaying hypoxemia during the apneic period that occurs after induction of general anesthesia. This will be evaluated by measuring the arterial oxygen tension (PaO2). The study will also evaluate whether there is any difference in PaO2 when using nasal prongs with flow rates of 5 L/minute versus 10 L/minute of oxygen.

NCT ID: NCT00740220 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Reproducibility of 6 Minute Walk Tests for Oxygen Desaturation

6MWT
Start date: September 2006
Phase: N/A
Study type: Observational

This trial will test the hypothesis that the 6 minute walk test (6MWT) is not reproducible as a measure for oxygen desaturation.

NCT ID: NCT00731510 Completed - Hypoxia Clinical Trials

MEDEX Hidden Valley 2008

Start date: June 2008
Phase: N/A
Study type: Interventional

During a multi−week expedition to the Himalaya, we aim to investigate i) whether dietary supplementation with carbohydrate drinks and gels can improve physical performance; and ii) the underlying mechanisms for any observed changes in performance. We hypothesise that i) carbohydrate supplementation will improve physical performance; and ii) the underlying mechanism of this improvement in performance will include maintenance of body glycogen (sugar) stores, prevention of dehydration and decrease in the incidence of acute mountain sickness.

NCT ID: NCT00675415 Completed - Hypoxemia Clinical Trials

Does Capnography Prevent Hypoxemia During Endoscopic Retrograde Cholangiopancreatography and Endoscopic Ultrasound?

Start date: September 2006
Phase: N/A
Study type: Interventional

Subjects undergoing elective ERCP and EUS will receive standard monitoring and sedation. In addition, capnography which measures carbon dioxide levels and can graphically assess respiratory activity will be used. Subjects will be randomized to either a capnography blinded or titration arm. In the capnography titration arm, the endoscopy team would be made aware of capnographic abnormalities as they arise throughout the procedure. In the capnography blinded arm, this information will not be available to the endoscopy team and represents standard of care. It is our hypothesis that using capnography can prevent low oxygen levels known as hypoxemia, during these procedures.

NCT ID: NCT00620711 Completed - Clinical trials for Hypoxic Ischemic Encephalopathy

Pilot Study of Head Cooling in Preterm Infants With Hypoxic Ischemic Encephalopathy

Start date: February 2008
Phase: Phase 1
Study type: Interventional

The hypothesis is that premature infants' can have enough cooling applied to cool their brain to decrease CNS injury without cooling their body.