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Altitude Sickness clinical trials

View clinical trials related to Altitude Sickness.

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NCT ID: NCT01587027 Completed - Mountain Sickness Clinical Trials

Safety Evaluation of Aminophylline and Methazolamide

Start date: December 2011
Phase: Phase 1
Study type: Interventional

This safety study is the first in a series of studies testing the application of the combination of aminophylline and methazolamide.

NCT ID: NCT01566565 Completed - Clinical trials for High Altitude Pulmonary Hypertension

The Safety Evaluation of Drug Combinations Against High Altitude Pulmonary Hypertension

Start date: March 2012
Phase: Phase 1
Study type: Interventional

This is a Phase I, three period, two sequence, open-label, randomized, crossover study, with the primary objective of testing the safety and tolerability of combined oral doses of theophylline and bambuterol in healthy human subjects. The secondary objective is to assess the pharmacokinetic profiles of theophylline and bambuterol when administered alone or in combination. It is hypothesized that the combination of these drugs is generally safe, and that no drug interaction can be observed.

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: NCT01530464 Completed - Clinical trials for High Altitude Pulmonary Hypertension

The Safety Evaluation of Aminophylline and Ambrisentan When Administered Orally Alone and in Combination to Healthy Volunteers

GQ01
Start date: February 2012
Phase: Phase 1
Study type: Interventional

This is a Phase I, three period, two sequence, open-label, randomized, crossover study, with the primary objective of testing the safety and tolerability of combined oral doses of aminophylline and ambrisentan in healthy human subjects. The secondary objective is to assess the pharmacokinetic profiles of theophylline (aminophylline) and ambrisentan when administered alone or in combination. It is hypothesized that the combination of these drugs is generally safe, and that no drug interaction can be observed.

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: NCT01519544 Completed - Clinical trials for High-altitude Sleep Disturbance

Comparison of Temazepam and Acetazolamide to Treat Difficulty Sleeping at High Altitude

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

More than 70% of visitors to high altitude suffer poor sleep. The present study seeks to answer the question: Which medication is associated with better sleep at high altitude: temazepam or acetazolamide? The investigators hypothesis is that one medication will be associated with higher subjective sleep scores than the other. The study will compare the sleep quality of 100 subjects as they take either temazepam or acetazolamide during a visit to high altitude.

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: NCT01465971 Completed - Clinical trials for Cheyne-Stokes Respiration

Monitoring of the Cerebral Tissue Oxygenation and Perfusion in the Adapting Climber During Sleep in High Altitude

PerOxySleep
Start date: May 2011
Phase: N/A
Study type: Observational

One of the major challenges in adapting to high altitudes is that with increasing altitude sleeping quality declines rapidly. Thus, the night sleep can only provide limited to none regeneration. It usually takes a prolonged stay at a constant altitude to adapt sufficiently to the altitude and to have a refreshing night sleep. 1975 Reit et. al showed in their EEG-recordings that the sleep architecture (the regular succession of the particular sleep phases) is disturbed by repeating arousals which occur due to an irregularity in the breathing rhythm. The purpose of this study is to create a better understanding of the underlying mechanisms that lead to failed acclimatization and AMS, due to sleep disturbance.

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.