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Acute Mountain Sickness clinical trials

View clinical trials related to Acute Mountain Sickness.

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NCT ID: NCT01842906 Completed - Clinical trials for Acute Mountain Sickness

Study Looking at End Expiratory Pressure for Altitude Illness Decrease (SLEEP-AID)

SLEEP-AID
Start date: October 2013
Phase: N/A
Study type: Interventional

The study is examining if an over-the-counter device (Theravent) worn while sleeping can reduce acute mountain sickness upon awakening in a high altitude trekking population.

NCT ID: NCT01794130 Completed - Clinical trials for Acute Mountain Sickness

The Incidence of Subclinical High-altitude Pulmonary Oedema at High Altitude

Start date: July 2011
Phase: N/A
Study type: Observational

The aim of this investigation is to determine the incidence of silent interstitial pulmonary edema by chest ultrasound at moderate altitude (3905m). Secondary endpoints are to detect a suspected association with acute mountain sickness (AMS), co-morbidities and endothelial dysfunction (marker of hypoxia responses, endothelial damage and inflammation).

NCT ID: NCT01698619 Recruiting - Clinical trials for Acute Mountain Sickness

Hemodynamic Changes in Altitude Adaptation

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

We use a new technology (Nexfin from BMEYE-Inventive Hemodynamics) to monitor Cardiac Output, Blood Pressure, Fluid Responsiveness, Pulse Oximetry, Hemoglobin Concentration, Oxygen Delivery in Climbers during their process of acclimatization on a expedition to Mount Aconcagua.

NCT ID: NCT01665781 Completed - Clinical trials for Acute Mountain Sickness

Erythropoietin in the Prevention of Acute Mountain Sickness

EPO-AMS
Start date: August 2012
Phase: Phase 4
Study type: Interventional

Acute mountain sickness (AMS) is a syndrome of nonspecific symptoms and is therefore subjective. The Lake Louise Consensus Group defined acute mountain sickness as the presence of headache in an unacclimatized person who has recently arrived at an altitude above 2,500 m plus the presence of one or more of the following: gastrointestinal symptoms (anorexia, nausea, or vomiting), insomnia, dizziness, and lassitude or fatigue. An increase in RBC mass is a natural feature of altitude acclimatization. Hypoxia-induced erythropoietin (EPO) secretion begins hours after ascent and stimulates bone marrow production of red blood cells, but this takes weeks to effect an increase in red cell mass . Therefore, it is feasible that EPO therapy weeks before altitude exposure decrease high altitude illness. In 1996, Young et al in U.S. Army Research Institute of Environmental Medicine (USARIEM) reported that autologous erythrocyte infusion did not ameliorate the decrement in maximal oxygen uptake at 4,300m altitude despite increasing arterial oxygen carrying capacity. On the basis of this report, USARIEM did not recommend use of recombinant EPO for altitude acclimatization. However, increases in erythrocyte count, hematocrit and hemoglobin associated with EPO therapy have been shown to decrease fatigue and increase work capacity and exercise tolerance. In addition, improvement in CNS function and cognitive ability has been noted with EPO therapy. Subjective benefits include improvement in sleep habits, tolerance to cold; decreased dyspnea, anginal symptoms and tachycardia and improved appetite, all of which are symptoms associated with high altitude illness. The investigators also reported improved muscle energy metabolism with EPO in dialysis patients, but not with RBC transfusion. In this study, the investigators will conduct a randomised controlled trial to assess the effect of EPO administration on AMS at an altitude of 4,130 m.

NCT ID: NCT01565603 Active, not recruiting - Clinical trials for Acute Mountain Sickness

Sleep and Cerebral Responses to High Altitude

VALLOT 2011
Start date: July 2011
Phase: N/A
Study type: Observational

Mechanisms underlying high-altitude intolerance as well as exercise performance limitation in hypoxia still remain to be fully understood. Recent data suggest that sleep disturbances on one hand and cerebral perturbations on teh other hand may be key mechanisms. The investigators evaluated 12 healthy subjects at sea level and at 4400 m of altitude for 7 days in order to better describe sleep and cerebral responses. The investigators hypothesized that sleep and cerebral disturbances play a critical role for the developement of acute mountain sickness and for exercise performance limitation during acute high-altitude exposure.

NCT ID: NCT01536288 Completed - Clinical trials for Acute Mountain Sickness

Can Rhodiola Crenulata Intake Improve Oxygen Saturation and Decrease the Incidence of Acute Mountain Sickness

Start date: October 2010
Phase: Phase 2
Study type: Interventional

Traditional folk medicine in the Arctic and Himalayan areas used Rhodiola species to enhance physical endurance, prevent aging, resist acute mountain sickness (AMS), and to treat fatigue, depression, anemia, impotence and respiratory infections. Rhodiola crenulata are widely used to prevent AMS in Himalayan areas and Lhasa in Tibet but none was examined by human study. The investigators conducted a randomized, double blind, placebo controlled, crossover study to investigate the efficacy of Rhodiola crenulata in preventing AMS.

NCT ID: NCT01522326 Completed - Clinical trials for Acute Mountain Sickness

Comparison of Metoclopramide and Ibuprofen for the Treatment of Acute Mountain Sickness

Start date: March 1, 2012
Phase: N/A
Study type: Interventional

The objective of this study is to determine the efficacy of metoclopramide in relieving the symptoms of Acute Mountain Sickness (AMS). It is our hypothesis that the combined antiemetic and analgesic effects of metoclopramide (which has been study-proven to be effective in relieving symptoms of migraine headache) will prove to be more efficacious in relieving symptoms of acute mountain sickness than the standard, previously-studied analgesic medication, ibuprofen.

NCT ID: NCT01468194 Completed - Clinical trials for Acute Mountain Sickness

Change in Peripheral Oxygen Saturation by Using Different Breathing Procedures in High Altitude

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

In this investigation the researchers explore whether different types of breathing procedures can improve the peripheral oxygen saturation to reduce the risk of becoming a acute mountain sickness or a high altitude pulmonary edema.

NCT ID: NCT01436383 Completed - Oxidative Stress Clinical Trials

Oxidative Stress in Hypobaric Hypoxia

Start date: March 2005
Phase: N/A
Study type: Interventional

The trial investigates changes in metabolism during high altitude expedition up to 6865m. A mass-spectrometry based platform is used to detect different oxidative stress related metabolites. Symptoms of acute mountain sickness are evaluated and correlated with laboratory parameters.

NCT ID: NCT01418157 Completed - Clinical trials for Acute Mountain Sickness

A Trial of Acetazolamide Versus Placebo in Preventing Mountain Sickness During Rapid Ascent

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

Acute mountain sickness is a common ailment in people venturing over 2500 m altitude. Pilgrims to high altitudes are at an added risk since they are unaware and they gain height faster than the recommendations. Acetazolamide is the standard treatment and prophylaxis of acute mountain sickness. There are no randomized controlled trials that have studied protective effects of Acetazolamide in rapid ascent, and there are few conflicting studies regarding this matter. This study is a randomized, double blinded, placebo controlled trial of Acetazolamide versus placebo in 380 healthy individuals travelling to Gosaikunda Lake of Nepal in rates of ascent that are faster than the recommendations. Acetazolamide 125 mg twice daily and a placebo will be randomly assigned for 3 days and participants will be assessed at 3 stations. This study will undertake to establish the role of Acetazolamide in Rapid Ascent and will be the first RCT done in this issue. The investigators hypothesize that Acetazolamide 125mg twice daily given before rapid ascent to high altitude in Nepalese pilgrims will not be superior to placebo in decreasing both the incidence and severity of acute mountain sickness.