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Hypoxia clinical trials

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NCT ID: NCT03806816 Recruiting - Clinical trials for Hypoxic-Ischemic Encephalopathy

Use of Melatonin for Neuroprotection in Asphyxiated Newborns

MELPRO
Start date: December 13, 2018
Phase: N/A
Study type: Interventional

Protection of brain development is a major aim in the Neonatal Intensive Care Unit. Hypoxic-Ischemic Encephalopathy (HIE) occurs in 3-5 per 1000 births. Only 47% of neonates have normal outcomes. The neurodevelopmental consequences of brain injury for asphyxiated term infants include cerebral palsy, severe intellectual disabilities and also a number of minor behavioural and cognitive deficits. However, there are very few therapeutic strategies for the prevention or treatment of brain damage. The gold standard is hypothermic treatment but, according to the literature, melatonin potentially acts in synergy with hypothermia for neuroprotection and to improve neurologic outcomes. Melatonin appears to be a good candidate because of its different protective effects including reactive oxygen species scavenging, excitotoxic cascade blockade, modulation of neuroinflammatory pathways. The research study will evaluate the neuroprotective properties and the effects of Melatonin in association with therapeutic hypothermia for hypoxic ischemic encephalopathy.

NCT ID: NCT03802175 Recruiting - Hypoxemia Clinical Trials

The Application Of Lung Ultrasound In Postoperative Hypoxemia Patients

Start date: January 10, 2019
Phase:
Study type: Observational [Patient Registry]

Postoperative hypoxemia was persistent and common after surgery.Rapid diagnosis and subsequent therapeutic measures must be adopted by anesthesiologists.Lung ultrasound has been confirmed to be more sensitive and accurate for diagnosis of pulmonary ailment than chest radiography.The primary objective of the present study was to evaluate lung complications by bedside lung ultrasonography on patients suffered from hypoxemia after general anesthesia in the postoperative period.

NCT ID: NCT03797482 Recruiting - Clinical trials for Breast Cancer Female

A Prospective Evaluation of the Peri-operative Hypoxia in Breast Cancer

Hypoxia
Start date: November 27, 2017
Phase:
Study type: Observational

To understand the effects induced by acute hypoxia that sets in during surgery in breast cancer. To study this, clinical samples (Tumor biopsies) will be obtained during the surgery after partial devascularisation (sample B) and stored for future genomic and proteonomic evaluations.

NCT ID: NCT03797300 Completed - Hypoxia Clinical Trials

Pulse Oximeter and Respiratory Rate Test

Start date: December 12, 2018
Phase: N/A
Study type: Interventional

Assessment of Spry Health's Loop oximetry accuracy in profound hypoxia Assessment of Spry Health's Respiratory rate accuracy in normal conditions and profound hypoxia

NCT ID: NCT03774043 Recruiting - Clinical trials for Spinal Cord Injuries

Timing and Dosage of Acute Intermittent Hypoxia in Persons With SCI

Start date: May 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This study will utilize short duration and mild levels of reduced oxygen (hypoxia) to induce spinal plasticity while evaluating the appropriate timing schedule for this intervention, as well as, the effects of superimposing sessions of a therapy, in individuals with chronic incomplete SCI. Our aim is to establish the time-course of outcome improvement and decay following a single session or multiple sessions of AIH therapy.

NCT ID: NCT03752749 Completed - Clinical trials for Spinal Cord Injuries

Impact of Intermittent Hypoxia and Prednisolone on Motor Performance in Persons With SCI

Start date: December 1, 2014
Phase: N/A
Study type: Interventional

The objective of this study is to examine the effects of mild acute intermittent hypoxia (AIH) in combination with an anti-inflammatory drug (i.e. prednisolone) on motor performance in persons with spinal cord injury (SCI).

NCT ID: NCT03750747 Recruiting - Hypoxemia Clinical Trials

Assessing the Feasibility and Effectiveness of Introducing Pulse Oximetry in IMCI Services

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to assess the feasibility, acceptability and operational challenges of introducing Pulse Oximeter (PO) in IMCI services to manage acute respiratory infections at first-level primary care facilities in Bangladesh (phase 1). The investigators will also evaluate the effectiveness and cost-effectiveness of introducing PO in IMCI services at first level primary care health facilities (phase 2). This study will employ a cluster randomized controlled trial design to evaluate the effectiveness of introducing PO in IMCI services (phase-2 objective). The feasibility assessment (phase-1 objective) will be nested within the larger effectiveness trail as internal piloting; which will help in generating evidence for designing a robust phase-2 trial. First-level primary healthcare facilities providing IMCI services will be regarded as clusters and the unit of randomization. Sixteen first level primary care health facilities (UH&FWC) will be randomly assigned to comparison and intervention facilities.

NCT ID: NCT03743610 Completed - Altitude Hypoxia Clinical Trials

Physiological Adaptations to Simulated Intermittent Altitude on Human Health and Performance

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The investigators expect to find that different intensity and altitude exposure levels will show what kind of intermittent exposure protocol is more beneficial to athletes and healthy individuals that experience acute exposure to altitude during exercise. This may furthermore be related to acute altitude exposure for recreational exercise use as well.

NCT ID: NCT03741998 Recruiting - Hypoxia Clinical Trials

Nasopharyngeal Airway Facilitate Transnasal Humidified Rapid Insufflation Ventilatory Exchange

Start date: November 7, 2018
Phase: N/A
Study type: Interventional

For performing transnasal humidified rapid insufflation ventilatory exchange (THRIVE), jaw-thrust maneuver have to maintain to make sure the airway open and the CO2 clearance during apnoea. The objective of present study is to prove that nasopharyngeal airway facilitate THRIVE and no need jaw-thrust maneuver and maintain the similar PO2 and PCO2 during apnoea.

NCT ID: NCT03738345 Completed - Hypoxemia Clinical Trials

The Effects of Flow Settings During High Flow Nasal Cannula for Adult Hypoxemia Patients

Start date: December 26, 2018
Phase: N/A
Study type: Interventional

High flow nasal cannula (HFNC) delivers oxygen at a flow which exceeds the patient's inspiratory flow demand in order to improve oxygenation. Numerous randomized control trials and meta-analyses have shown that HFNC improves oxygenation and helps avoid intubation in hypoxemic patients, as well as reduce work of breathing, improve ventilation, and decrease hypercapnia in COPD patients. Flow settings play a critical role when using HFNC, as increased flow can reduce inspiratory effort, improve ventilation, and dynamic lung compliance. However, flow rates used in many studies vary widely. The clinical effects of different HFNC flow setting, specifically to match or over than a patients' own inspiratory flow, is still unknown.