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Hypoxemia clinical trials

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NCT ID: NCT01477450 Completed - Hypoxemia Clinical Trials

Comparison of Oxygen Delivery Devices for Reversal of Altitude-Induced Hypoxemia in Normal Subjects

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

This study will compare the ability of pulsed-dose oxygen from a concentrator to reverse altitude-induced hypoxemia compared to compressed gas from a standard oxygen cylinder.

NCT ID: NCT01470170 Completed - Hypoxemia Clinical Trials

Regimen of Alfentanil in Propofol Sedative Fibro-bronchoscopy

Start date: October 2010
Phase: Phase 4
Study type: Interventional

Alfentanil (Alf) is used in combination with Propofol (Pro) in fiber-bronchoscopy and in many other conscious sedation procedures. Alf and Pro have the characteristic of rapid anesthetic onset and quick recovery, synergic sedative effect and unwanted side effects too. However, the amount of Alf needed in combination with Pro for induction and the timing of administration was no standardized. The investigators designed this study to evaluate the optimal regimen, dose and timing of Alf in Target-Controlled infusion (TCI) of Pro for flexible bronchoscopy sedation, and also to evaluate the influence of variable regimen of Alf and Pro on hypoxemia, hypotension, cough severity, and Pro injection related pain.

NCT ID: NCT01457651 Completed - Hypoxemia Clinical Trials

Comparison of Four Different Recruitment Maneuvers in Patients After Coronary Surgery

RECR-CABG
Start date: March 2010
Phase: N/A
Study type: Interventional

The risk of respiratory failure after cardiac surgery is high, and it may result in many complications. The maneuver of alveolar recruitment may improve the oxygen transport in the human organism. The investigators compare three different types of alveolar recruitment in patient after cardiac surgery, to reveal which one is better.

NCT ID: NCT01377051 Completed - COPD Clinical Trials

Effect of Indacaterol Maleate in Chronic Obstructive Pulmonary Disease (COPD) on Lung Volume and Related Dyspnea

Start date: May 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether indacaterol maleate 300 micrograms (mcg) is effective in the acute treatment of COPD and in particular on reducing lung hyperinflation and dynamic volumes.

NCT ID: NCT01085539 Completed - Hypoxemia Clinical Trials

Oxygen Saturation Alarms in the Neonatal Intensive Care Unit

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

Infants will be observed in the neonatal intensive care unit for 4 hours. The observer will note the timing of oxygen saturation alarms, staff response, and interrupted staff activities.

NCT ID: NCT01072487 Completed - Hypoxemia Clinical Trials

Capnography During Colonoscopy

ColoCap
Start date: February 2010
Phase: Phase 3
Study type: Interventional

In the study the value of capnography for avoiding complications during sedation for colonoscopy is evaluated.

NCT ID: NCT01072474 Completed - Hypoxemia Clinical Trials

Capnography During ERCP

EndoBreath
Start date: February 2010
Phase: Phase 3
Study type: Interventional

In the study the value of capnography for avoiding complications during sedation for ERCP is evaluated.

NCT ID: NCT01069185 Completed - Cardiac Arrest Clinical Trials

Differences in Morbidity Between a Necessity Endotracheal Suctioning Protocol Versus a Routine Endotracheal Suctioning

Start date: February 2010
Phase: N/A
Study type: Interventional

Morbidity frequency associated to a endotracheal suctioning is different between a necessity endotracheal suctioning protocol versus a routine endotracheal protocol.

NCT ID: NCT01014299 Completed - Hypoxemia Clinical Trials

Recruitment Maneuver After Intubation

Start date: December 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of a recruitment maneuver immediately after intubation in hypoxemic patients.

NCT ID: NCT00896584 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Exercise Pulseoximetry for Pre-flight Evaluation of Chronic Obstructive Pulmonary Disease (COPD) Patients

Start date: May 2009
Phase: N/A
Study type: Observational

Some patients with chronic obstructive pulmonary disease (COPD) need supplementary oxygen during air travel. Guidelines issued by The British Thoracic Society (BTS) for pre-flight evaluation do not discriminate sufficiently between those who need supplementary oxygen during flight, and those who can do without. Previous studies have indicated that decreasing hemoglobin oxygen saturation during exercise may predict in-flight hypoxemia. The objective of the present study is to examine if adding exercise oxygen desaturation to the BTS algorithm will better predict requirements for in-flight supplementary oxygen.