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Hypoxia clinical trials

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NCT ID: NCT05463042 Completed - Clinical trials for Intermittent Hypoxia

Intermittent Hypoxia and Balance Control

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

This study aims to determine the effect of acute mild intermittent hypoxia on ankle plantarflexor muscle output during balance regulation and walking in younger and older adults. Fifteen younger adults and 15 older adults will be recruited to participate in the cross-over design study that requires 2 visits (at least 1-week apart). Participants will be pseudo-randomly assigned to receive either intermittent hypoxia or sham during the first visit, and then switch over to receive sham or intermittent hypoxia during the 2nd visit. Muscle activation patterns and kinetic and kinematics during standing and walking will be recorded before and after the intermittent hypoxia/sham. It is hypothesized that compared to the sham condition, both younger and older participants will show greater increases in ankle plantarflexor muscle activation during gait and balance assessments following intermittent hypoxia.

NCT ID: NCT05462834 Not yet recruiting - Glucose Intolerance Clinical Trials

Impact of Nocturnal Hypoxemia on Glucose in High Altitude Sleep Disordered Breathing

Start date: September 1, 2024
Phase: N/A
Study type: Interventional

Sleep disordered breathing is associated with impaired glucose tolerance and incident diabetes. Nocturnal hypoxemia is a potential stimulus of glucose intolerance. It is especially severe and highly prevalent in high altitude residents. Intervening on nocturnal hypoxemia may therefore improve glucose control and decrease the public health burden in high altitude populations. The objective of this study is to examine the impact of hypoxemia on glucose homeostasis in high altitude residents. The investigators will address this objective by examining the effect of supplemental oxygen on glucose in a randomized cross-over study.

NCT ID: NCT05447416 Recruiting - Clinical trials for Healthy Active Athletes

Intermittent Hypoxic Training (IHT) Versus Hyperbaric Oxygen Therapy (HBOT) for Aerobic Performance

Start date: June 1, 2023
Phase: N/A
Study type: Interventional

Comparing the effect of HBOT and IHT on aerobic performance of athletes.

NCT ID: NCT05441007 Enrolling by invitation - Hypoxia Clinical Trials

The Effect of Hypercapnia on Physiological Parameters During Short-term Breathing

HYPERCO
Start date: June 26, 2022
Phase: N/A
Study type: Interventional

The aim of the project is to evaluate the effect of hypercapnia on physiological parameters in a healthy person during short-term hypoxia and hypercapnia.

NCT ID: NCT05439239 Recruiting - Hypoxia Clinical Trials

Effects of Hypoxic Repeated Sprint Training on Performance in Normoxia in Male and Female Athletes

RSHwomen
Start date: April 21, 2022
Phase: N/A
Study type: Interventional

With the increased participation of women in sports, it is essential to develop gender-tailored training strategies for improving exercise performance. Males and females exhibit gender-specific characteristics and they therefore respond differently to physical exercise. Improving repeated sprint ability (RSA, i.e., ability to perform repeated short duration sprints separated by brief recovery intervals) in women is important for sports performance, as it is a key factor in most team and racket sports. Repeated sprint training in hypoxia is increasingly popular in this field, as it has demonstrated further improvements in sea-level repeated sprint performance than similar training in normoxia. However, these observations are based mainly on male athletes. Whether the effects of hypoxic repeated sprint training on repeated sprint performance in normoxia differ between genders is not yet known, therefore the investigators propose to examine those possible differences in this study. The aim of this study is to investigate whether the effects of hypoxic repeated sprint training on repeated sprint performance in normoxia differ between males and females who participate in team/racket sports. Considering the sex-specific characteristics that males and females exhibit, the investigators hypothesize that after 7 weeks of hypoxic repeated sprint training the improvements in repeated sprint ability at sea level will be greater in males than in females. To answer this question, the investigators will measure the following: body composition (lean body mass); body weight and height; VO2max; blood (estrogen, lactate, hemoglobin, hematocrit); repeated sprint ability (RSA) test; muscle oxygenation (concentrations for oxyhemoglobin, deoxyhemoglobin, and total hemoglobin/myoglobin); 30-s Wingate test; heart rate (HR); power output; rate of perceived exertion (RPE); visual analogue scale (VAS; pain level in legs). The investigators will recruit 48 volunteers and they will randomly assign them into the normoxic or hypoxic training group, without giving any information about their group. The volunteers should meet the following inclusion criteria: females (on monophasic oral contraceptive pill) and males, age between 18-40 years, recreationally participating in team/racket sports min 3h/week with at least 2 years of experience prior to the study. Exclusion criteria will be: smoking, exposure to altitude >1500 m one month before the study, any health conditions or injuries that could compromise the participant's safety during training/testing, prescribed medication, performing repeated sprint training more than once per week. Males and females, matched for VO2max and sprint performance, will perform repeated sprint training (3 sets during week 1-6, 2 sets during week 7 with 5min active recovery in between, 5 x 10s maximal sprints with 20s active recovery in between) in hypoxia or normoxia 2x/week for 7 weeks. Before and after the training period, the following tests and measurements will be performed: body composition analysis, VO2max test, blood sampling for measuring hemoglobin and estrogen concentrations and hematocrit, determination of hemoglobin mass, RSA test, muscle oxygenation assessment during RSA test, 30-s Wingate test and blood lactate measurements.

NCT ID: NCT05433155 Recruiting - Hypoxia Clinical Trials

Nasotracheal Intubation With VL vs DL in Infants Trial

NasoVISI
Start date: June 6, 2022
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT05430724 Completed - Hypotension Clinical Trials

The Effects of Nicardipine and Esmolol Applied for Controlled Hypotension

Start date: May 12, 2022
Phase: N/A
Study type: Interventional

In this study, the effects of nicardipine and esmolol applied for controlled hypotension in rhinoplasty on hemodynamics and regional renal oxygenation will be investigated.

NCT ID: NCT05423470 Completed - Clinical trials for Intermittent Hypoxia

Effect of Intermittent Hypoxia on Ischemia-reperfusion Injury in Healthy Individuals

Start date: May 30, 2019
Phase: N/A
Study type: Interventional

The objective of the present study is to determine whether intermittent hypoxia protects against ischemia-reperfusion injury in young and older healthy individuals. The investigators hypothesize that intermittent hypoxia will attenuate the reduction in flow-mediated dilation following ischemia-reperfusion injury.

NCT ID: NCT05422430 Recruiting - Hypoxemia Clinical Trials

Rebreathing-induced Hypoxia and Glucose Levels

Start date: October 21, 2021
Phase: N/A
Study type: Interventional

The aim of this research project is to determine the effect of repeated maximal voluntary apneas on glucose uptake during an oral glucose tolerance test in healthy individuals, individuals with prediabetes and patients with type 2 diabetes.

NCT ID: NCT05417217 Recruiting - Clinical trials for Coronary Artery Disease

The Effect of Continued Mechanical Ventilation on the Occurrence of Myocardial Ischemia

VENTMICS-II
Start date: October 17, 2022
Phase: N/A
Study type: Interventional

The goal of this study is to examine the influence of mechanical ventilation on the occurrence of myocardial ischemia in patients undergoing endo-CABG.