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Hypoxia clinical trials

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NCT ID: NCT01816607 Completed - Rectal Neoplasms Clinical Trials

Functional MRI of Hypoxia-mediated Rectal Cancer Aggressiveness

OxyTarget
Start date: October 2013
Phase:
Study type: Observational

The purpose of this study is to establish a reliable method for detection of rectal cancer patients with aggressive tumor at risk of metastatic disease and death by functional MRI.

NCT ID: NCT01795534 Completed - Hypoxia Clinical Trials

Beetroot Juice as a Potential Ergogenic Aid During Exercise in Hypoxia

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

The study will aim to describe and evaluate the effect of beetroot juice supplementation upon whole body running exercise at altitude. It is hypothesised that beetroot supplementation will decrease time to complete a 10 km time trial.

NCT ID: NCT01793129 Completed - Infant, Newborn Clinical Trials

Preemie Hypothermia for Neonatal Encephalopathy

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

This study is a randomized, controlled trial to assess safety and effectiveness of whole body hypothermia for 72 hours in preterm infants 33-35 weeks gestational age (GA) who present at <6 hours postnatal age with moderate to severe neonatal encephalopathy (NE). The study will enroll infants with signs of NE at 18 NICHD Neonatal Research Network sites, and randomly assign them to either receive hypothermia or participate in a non-cooled control group.

NCT ID: NCT01732146 Completed - Clinical trials for Hypoxic Ischemic Encephalopathy

Efficacy of Erythropoietin to Improve Survival and Neurological Outcome in Hypoxic Ischemic Encephalopathy

Neurepo
Start date: March 28, 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the efficacy of high dose Erythropoietin to improve survival and neurologic outcome in asphyxiated term newborn undergoing cooling.

NCT ID: NCT01725464 Completed - Hypoxia Clinical Trials

The Effect of Nasal Cannula During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy

Start date: November 2012
Phase: Phase 4
Study type: Interventional

During early postoperative after lung resection surgery, patients without oxygen supplementation may experience hypoxemia. Oxygen supplementation can be given via oxygen mask or cannular. In this study the investigators want to the sudy the effect of oxygen supplementation via oxygen cannular during the first 120 minutes after surgery

NCT ID: NCT01700088 Completed - Hypoxia Clinical Trials

The Effect of Nasal Cannulae During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy

Start date: November 2012
Phase: N/A
Study type: Observational

At our institute,during the first 2 hour postoperative, we used to give supplement oxygen via face mask in patient having lung resection surgery. After then if the patient is fine, we'll replace the face mask with nasal cannular untie the next morning. We hypothesized that oxygen mask can be replace by nasal cannular without any hypoxia.

NCT ID: NCT01689090 Completed - Clinical trials for Diabetes Mellitus Type 1

Diameter Changes of Retinal Vessels During Hypoxia

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

The primary objective is to study if an inhibition of nitric oxide and/or prostaglandins affect the diameter changes of retinal vessels observed during hypoxia. Diameter changes are studied using the Dynamic Vessel Analyzer.

NCT ID: NCT01650974 Completed - Hypoxia Clinical Trials

High Flow Nasal OXygen Therapy in High Risk Patients of Hypoxia Undergoing Diagnostic BRONCHOscopy

HFNOT
Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of nasal high flow oxygen therapy during diagnostic bronchoscopy.

NCT ID: NCT01638793 Completed - Hypoxia Clinical Trials

Capnographic Monitoring of Propofol-sedation During Colonoscopy

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

The present study is a randomized, prospective, single-blinded study. Patients presenting for colonoscopy under sedation will be included according to the statistical sample size calculation. Patients will be randomized to either group 1- capnographic monitoring or group 2- oxygenic monitoring during Propofol-based sedation for colonoscopy. Episodes of Hypoxia are documented and compared in both groups.

NCT ID: NCT01620203 Completed - Clinical trials for Intraventricular Hemorrhage

Observational Study in Preterm Infants With Intracranial Hemorrhage

Start date: June 2012
Phase:
Study type: Observational

Intracranial Hemorrhage (ICH) is an important morbidity affecting premature infants and can have considerable effects on neurodevelopmental outcome. The investigators showed that preterm infants with severe ICH have decreased cerebral oxygenation several weeks after the hemorrhage. The mechanisms involved in this state of decreased cerebral oxygenation in preterm infants and the effects on cerebral function are unknown. This longitudinal observation study will evaluate physiologic parameters to determine trends in cerebral oxygenation and function in preterm infants with ICH in comparison to infants without ICH.