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Hypoxia clinical trials

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NCT ID: NCT02642705 Recruiting - Obesity Clinical Trials

High Intensity Interval Training and Hypoxic Conditioning in Obese Patients

HYPINT
Start date: September 2015
Phase: N/A
Study type: Interventional

The present study aims at evaluating the effect of two innovative treatment strategies in obese patients: high intensity interval training and hypoxic conditioning. Obese patients will be randomized in groups performing high intensity interval training, constant load training, hypoxic conditioning or placebo normoxic conditioning for 8 weeks. The effects of the interventions will be measured regarding exercise tolerance, blood pressure, body composition, metabolic status.

NCT ID: NCT02589691 Recruiting - Hypoxemia Clinical Trials

Neuromuscular-Blocking Agents and Hypoxemia During Intubation in Infants (ROC-HYPOX)

ROC-HYPOX
Start date: December 23, 2015
Phase: Phase 4
Study type: Interventional

The prevention of the occurrence of respiratory events is a constant concern in pediatric anesthesia, as these represent the main cause of the anesthesic mortality. These events occur partly during induction of anesthesia and are all the more frequent as the child is young. The French recommendations do not propose the use of neuromuscular-blocking agents in pediatric anesthesia. This recommendation is controversial In a recently published study, it has been shown that the use of neuromuscular blocking agents during induction in children under 2 years improves intubating conditions and reduces the incidence of hemodynamic and respiratory events. This monocentric study, centered on intubating conditions, does not allow to conclude on the influence of muscle relaxants on reduction of the respiratory morbidity. The objective of study is to demonstrate that, in children under 2 years, changing the anesthesia protocol can reduce the incidence and severity of episodes of hypoxemia associated with respiratory events occurring during induction

NCT ID: NCT02460653 Recruiting - Hypoxia Clinical Trials

Effects of High Flow Nasal Cannula on Deadspace Reduction and Regional Distribution of Ventilation

HFNC
Start date: May 1, 2015
Phase: N/A
Study type: Interventional

1. To determine the lowest nasal cannula flow rate in which upper airway deadspace is reduced. Hypothesis - The lowest flow rate of high flow nasal cannula (HFNC) will reduce upper airway (extrathoracic) deadspace and improve respiratory efficiency by reducing transcutaneous CO2 and/or lower respiratory rate. 2. To determine the lowest nasal cannula flow rate in which regional distribution (as defined by EIT) of ventilation changes. Hypothesis - Moderate to high flow rates will create positive pressure that leads to improved regional distribution of ventilation.

NCT ID: NCT02436018 Recruiting - Gastric Cancer Clinical Trials

WEI NASAL JET for The Sedation of Outpatient Upper Gastrointestinal Endoscopy

Start date: March 2015
Phase: N/A
Study type: Interventional

Low pulse oximetry is the most common adverse events during sedation for upper gastrointestinal endoscopy. The main reason is the glossoptosis after sedation. In present study a new designed nasopharyngeal airway embedded with jet ventilation catheter(WEI NASAL JET) will be utilized in order to reduce the hypoxia. At the same time the safety will be evaluated.

NCT ID: NCT02287220 Recruiting - Hypoxia Clinical Trials

Non Contact Measurement of Vital Signs

Start date: November 2014
Phase:
Study type: Observational

The purpose of this study is to test the accuracy of a web cam-based biomedical device developed at UVA (not FDA-approved) that is designed to measure heart rate, respiratory rate, and oxygen saturation without requiring any patient contact. One potential application of such a device would be in the field of infant monitoring allowing parents (and physicians) to monitor the vital signs of infants continuously. The investigators therefore propose to record the heart rate, respiratory rate, and oxygen saturation of 100 infants (defined as children aged 12 months or less) who are receiving continuous oxygen, heart rate, and respiratory rate monitoring with a traditional vital signs monitor. The relationship between "non-contact" and "gold standard" (GE monitoring equipment) heart rate, respiratory rate, and oxygen saturation will be analyzed using regression and limits of agreement analysis.

NCT ID: NCT01994785 Recruiting - Hypotension Clinical Trials

Use of Capnography in EGD and Colonoscopy With Moderate Sedation.

Start date: November 2013
Phase: N/A
Study type: Interventional

This study will provide capnography monitoring during routine upper endoscopy and colonoscopy with moderate sedation in order to see if it improves safety.

NCT ID: NCT01814449 Recruiting - Breast Cancer Clinical Trials

Relationship Between Hypoxia and Endocrine Response in Human Breast Cancer

Start date: March 2012
Phase: N/A
Study type: Observational [Patient Registry]

The aim of our current study was to analyze whether 18F-labeled Fluoromisonidazole (1-(2-nitro-1-imidazolyl)- 2-hydroxy-3-fluoropropane [18F-FMISO]) PET/CT and expression of HIF-1-alpha could predict response of primary endocrine therapy in ER-positive breast cancer

NCT ID: NCT01627652 Recruiting - Hypoxia Clinical Trials

Human Adaptation to High Altitude

Start date: April 2012
Phase: N/A
Study type: Interventional

This scientific study aims at studying human adaptations to high altitude and the studies will be conducted at the University of Zürich and during a 4 week high altitude "expedition" to the Jungfraujoch research station at 3450 m altitude. The proposal is made up of several independent biological research projects to be conducted in the same healthy volunteers participating in the study. Thus, the subjects will be studied at sea level, and then during 4 weeks of acclimatization to high altitude, and for some experimental purposes all subjects will also be studied one and two weeks after return to sea level.

NCT ID: NCT01619280 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Safety Study of Nebulized Sodium Nitroprusside in Adult Acute Lung Injury

Start date: May 2012
Phase: Phase 1
Study type: Interventional

Acute lung injury (ALI) is caused by a wide variety of conditions, but always characterized by hypoxia and non-cardiogenic pulmonary edema. Current treatment of ALI is supportive and treatment of the underlying cause. New therapies to treat severe ALI have not been shown to improve survival, and are limited by financial and logistical resources. The investigators propose to investigate the role of inhaled sodium nitroprusside (iSNP) in ALI. Sodium nitroprusside (SNP) is a vasodilator. When inhaled, SNP may travel to areas of the lung participating in gas exchange, and cause the blood vessels surrounding these areas to enlarge. This may result in an increase of blood vessels to these areas of the lung, and improve oxygenation. Currently, iSNP has not been studied in the adult population. Therefore, this study is intended to find the safety profile of varying doses of iSNP.

NCT ID: NCT01567800 Recruiting - Prostate Cancer Clinical Trials

Prostate Hypoxia FAZA

Start date: April 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to look for low levels of oxygen (hypoxia) in prostate cancer using a special x-ray test called a positron emission tomography (PET)scan. Hypoxia may have an effect on how prostate cancer grows and responds to treatments like radiotherapy and chemotherapy. The use of PET scans to measure hypoxia may be better and simpler than the methods used previously.