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Hypoxia clinical trials

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NCT ID: NCT03009643 Recruiting - Hypoxemia Clinical Trials

Salvage Treatment of Inhaled Nitric Oxide in Patients With Refractory Hypoxemia After Aortic Surgery

Start date: October 2016
Phase: N/A
Study type: Interventional

Hypoxemia is a common complication after aortic surgery. As this complication has an adverse effect on the postoperative course of the patient, early treatment is important; however, the mechanism of hypoxemia after surgery for acute aortic dissection remains unclear. Recently, the investigators found that inhaled Nitric Oxide can improve the oxygenation in some of these patients. The investigators are trying to evaluate the effectiveness and safety of inhaled Nitric Oxide in patients with refractory hypoxemia after aortic surgery.

NCT ID: NCT03000686 Terminated - Healthy Volunteers Clinical Trials

Study of GSK2586881 on Acute Hypoxia and Exercise

Start date: May 17, 2017
Phase: Phase 1
Study type: Interventional

This study is conducted to examine how GSK2586881, a recombinant human ACE2 peptide, modulates the acute hypoxic pulmonary vasoconstriction (HPV) response in healthy volunteers. The study will be single-center, randomized, placebo-controlled and double blind (sponsor open). Subjects will be randomized to receive a single intravenous (IV) dose of GSK2586881 or placebo (saline) in a crossover design. The primary objective of the study is to evaluate the effect of a single IV dose of GSK2586881 on the HPV response in healthy volunteers during exercise under hypoxic conditions. Approximately 35 subjects will be enrolled for a maximum of 56 days.

NCT ID: NCT02989168 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis

Study to Evaluate the Effect of GBT440 Administered to Subjects With IPF on Supplemental Oxygen at Rest

Zephyr
Start date: November 2016
Phase: Phase 2
Study type: Interventional

This is an open label study in which eligible IPF subjects who are using supplemental oxygen at rest will receive GBT440 orally daily.

NCT ID: NCT02984657 Completed - Hypoxia Clinical Trials

Reverse Trendelenburg Positioning and Its Effect on Outcomes: a Retrospective Study of Consecutive Patients

Start date: May 2015
Phase: N/A
Study type: Observational

The purpose of this study is to investigate whether intraoperative reverse Trendelenburg positioning decreases postoperative hypoxemia and perioperative pulmonary aspiration rates.

NCT ID: NCT02976883 Completed - Lung Cancer Clinical Trials

[18F]HX4 PET/CT Imaging for Detection of Hypoxia

OXYPET
Start date: March 31, 2015
Phase: Phase 2
Study type: Interventional

The aim of this study is to investigate the radiotracer [18F]HX4 for non-invasive detection of hypoxia in patients with head and neck, or lung cancer. Each participant will undergo a diagnostic [18F]HX4 PET/CT scan before beginning radiotherapy treatment. Patient follow up data will be collected from routine appointments, and analysed with the hypoxia scan results to assess whether [18F]HX4 PET/CT scanning can predict patient outcome from radiotherapy treatment.

NCT ID: NCT02976051 Recruiting - Radiotherapy Clinical Trials

DAHANCA 33: Image Guided Dose-escalated Radiotherapy to Patients With Hypoxic HNSCC

Start date: January 2017
Phase: Phase 2
Study type: Interventional

Aim: To improve curability of radiotherapy in HNSCC patients identified by hypoxic FAZA-PET scanning

NCT ID: NCT02973438 Completed - Obesity Clinical Trials

Effects of Intermittent Hypoxia (IH) on Metabolism and Dysglycemia, in Overweight/Obese Persons SCI

Start date: December 2016
Phase: N/A
Study type: Interventional

The purpose of this research is to examine changes in blood glucose control and metabolism in individuals with SCI and non injured controls at rest and during exercise after five days of exposure to IH. This response will be compared with breathing normal room air (a SHAM control).

NCT ID: NCT02966743 Withdrawn - Clinical trials for Cerebral Ischemia-Hypoxia

Effect of Sedatives on Regional Cerebral Oxygen Saturation

2
Start date: November 2016
Phase: N/A
Study type: Interventional

Compare the changes of regional cerebral oxygen saturation during midazolam or dexmedetomidine sedation for spinal anesthesia in the elderly patients who undergoing femur surgery.

NCT ID: NCT02966418 Completed - Clinical trials for Carotid Artery Stenosis

Hypoxic Preconditioning on Patients

Start date: January 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to study the effects of intermittent whole-body hypoxic preconditioning on patients with carotid artery stenosis.

NCT ID: NCT02961920 Completed - Hypoxia Clinical Trials

The Effect of Prolonged Inspiratory Time on Pulmonary Mechanics in Obese Patients

Start date: November 2016
Phase: N/A
Study type: Interventional

The area of aesthesia-induced atelectasis is much larger in the obese compared with the non-obese, but there may also be more airway closure and impaired matching of ventilation and lung blood flow. When an anesthetized patient is turned to the prone position, dynamic compliance (Cdyn) decreases and peak airway pressure increases unless the abdomen hangs freely to prevent the abdominal viscera from compromising the diaphragm movement. Although the Wilson frame is designed to allow the abdomen to hang, it partially compresses the anterior abdominal wall and therefore does not allow the abdomen to hang completely, especially in obese patients. This in turn increases peak airway pressure and decreases Cdyn, oxygenation. This study aimed to investigate the effects of a prolonged I:E ratio (i.e., 1:1) compared with the conventional I:E ratio of 1:2 on respiratory mechanics and hemodynamics during spine surgery in the prone position in obese patients. We hypothesized that, compared with an I:E ratio of 1:2, a ratio of 1:1 improve oxygenation without hemodynamic instability .