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Active clinical trials for "Hypoxia"

Results 41-50 of 998

Ultrasonographic Evaluation of the Diaphragm During NHF Versus NIV Use in Respiratory Failure

Diaphragm IssuesRespiratory Failure With Hypoxia2 more

This study will describe influence of NHF or NIV to different ultrasonographic parameters of the diaphragm. Therefor subjects will be randomized to the sequence NHF and than NIV or NIV and than NHF. In all subjects same parameters will be evaluated.

Recruiting6 enrollment criteria

HFNC Compared With Facial Mask in Patients With Chest Trauma Patients

Chest TraumaHypoxia

Guidelines for noninvasive ventilation (NIV) recommend continuous positive airway pressure in patients with thoracic trauma who remain hypoxic . However, no any suggestion was applied for high flow nasal cannula (HFNC). Therefore, Our aim was to determine whether HFNC reduces intubation in severe trauma-related hypoxemia.

Recruiting13 enrollment criteria

Improving Outcomes of Respiratory Patients With Exertional Hypoxemia

Pulmonary Rehabilitation

The primary aim of this pilot randomized controlled trial is to determine feasibility of the proposed pulmonary rehabilitation intervention.

Recruiting7 enrollment criteria

Automated Oxygen Titration at Home in Patients With COPD on Home Oxygen

COPDHypoxemia

Sixteen patients with COPD and long term oxygen treatment (LTOT) will be included in the study. An automated home oxygen titrations (HOT) device will be attached to the patient´s home oxygen equipment. For 2x4 consequent days, the patients will be monitored and saturations, oxygen flow and physical activity level will be registered. In randomized order, the patients will use their usual fixed oxygen dose or automated oxygen titration during the first four days and then crossover. The monitoring consists of a wrist pulse oximeter (register pulse and saturation which is send to the HOT device) and a physical activity sensor attached to the patient's knee. At study start and after both of the four days the patients´dyspnea and QoL will be assessed. After the study period the patients will in an explorative design based on qualitative methodology be interviewed in order to explore the patients experiences with automated oxygen titration during daily activity and on dyspnea.

Recruiting13 enrollment criteria

Automated Adjustment of Oxygen on Patient With Acute COPD Exacerbation - FreeO2 HypHop

Oxygen ToxicityCOPD Exacerbation3 more

The aim of this study is to evaluate if automated adjustment of oxygen (with FreeO2 device) can reduce the hospital length of stay for acute exacerbation of COPD with comparison of manual oxygen titration.

Recruiting14 enrollment criteria

Overcoming Chemoresistance in Advanced Ovarian Cancer Via Targeting Hypoxia

Epithelial Ovarian CancerFallopian Tube Cancer2 more

The goal of this non-randomized prospective study is to use 18F-EF5-PET/CT imaging to identify and locate intraabdominal hypoxic ovarian cancer lesions. With targeted surgical sampling, precisely obtain hypoxic and potentially chemoresistant cancer tissue for our analyses and identify key molecular differences between hypoxic and non-hypoxic tumors within the same patient. A portion of advanced stage EOC are inoperable at diagnosis and can be treated with neoadjuvant chemotherapy (NACT) before surgery. This approach offers a unique opportunity to study how hypoxic tumor areas respond to treatment.

Recruiting5 enrollment criteria

Sedation, Temperature and Pressure After Cardiac Arrest and Resuscitation

Cardiac Arrest With Successful ResuscitationHypoxia1 more

The STEPCARE-trial is a 2x2x2 randomised trial studying patients who have been resuscitated from cardiac arrest and who are comatose. It will include three different interventions focusing on sedation targets, temperature targets and mean arterial pressure targets.

Recruiting9 enrollment criteria

Nasotracheal Intubation With VL vs DL in Infants Trial

Intubation ComplicationIntubation; Difficult or Failed4 more

Nasotracheal Intubation with Videolaryngoscopy versus Direct Laryngoscopy in Infants (NasoVISI) Trial is a prospective randomized multicenter study. The study will be conducted at 8 centers in the United States. It is expected that approximately 700 subjects enrolled to product 670 evaluable subjects.The randomization is 1:1 naso tracheal intubation with the Storz C-Mac Video Videolaryngoscopy (VL) or the Standard Direct Laryngoscope (DL). The primary objective is to compare the nasotracheal intubation (NTI) first attempt success rate using VL vs. DL in infants 0-365 days of age presenting for cardiothoracic surgery and cardiac catheterizations.

Recruiting11 enrollment criteria

FreeDom: Innovative Strategy for the Management of COPD Exacerbations

Oxygen DeficiencyCOPD Exacerbation

The main objective of the study is to assess the "FreeDom" innovative strategy (FreeO2 at Domicile) to reduce hospitalization duration in patients with COPD exacerbation. This strategy associates early hospital discharge, automated O2 flow weaning with FreeO2 system, telemedicine and tele-rehabilitation. The main hypothesis of this study is that the FreeDom strategy will reduce the number of hospitalization day by 50 percent at day 30.

Recruiting15 enrollment criteria

Postoperative Hypoxia and Body Position

Postoperative ComplicationsAbdominal Surgery1 more

The study aims at investigate whether the oxygen partial pressure is improved in the prone position postoperative after abdominal surgery. Included are 50 adults operated with abdominal surgery. The Intervention is turning from supine to prone position and then back to supine position while measuring whether an improvement occurs in oxygen saturation and oxygen partial pressure, or not.

Recruiting4 enrollment criteria
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