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Clinical study on the effect of dexamethasone combined with stepwise deoxygenation therapy on the initial habituation of soldiers entering high altitude rapidly

Clinical study on the effect of dexamethasone combined with stepwise deoxygenation therapy on the initial habituation of soldiers entering high altitude rapidly

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122299
Enrollment
Unknown
Registered
2026-04-11
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute mountain sickness

Interventions

Dexamethasone group:The subjects took dexamethasone acetate tablets daily at a dose of 1.5mg/time, twice a day, followed by monitoring of vital signs and testing of habituation levels at different tim
Staged oxygen weaning group:The initial oxygen concentration of the subjects was 4L/min, and vital signs including blood pressure, heart rate, respiration, and oxygen saturation were measured every ha
Combined group:On the basis of stepwise deoxygenation, the subjects took dexamethasone acetate tablets daily at a dose of 1.5mg/time, twice a day, until reaching initial habituation.
Control group:The subjects did not undergo any intervention and underwent vital sign monitoring and habituation level testing at different time points. Check vital signs every half hour, including blo

Sponsors

General Hospital of Xizang Military Command of the Chinese People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Participants enter high-altitude areas (above 3000 meters above sea level) from plain areas (below 500 meters above sea level) within one week; 2. Participants need to live, work, or engage in high-intensity physical activities in high-altitude environments and have a need for high-altitude adaptation; 3. No serious heart, lung, circulatory, or nervous system diseases; 4. Within the age range of 18-65 years old; 5. Participants need to understand the research purpose, process, and potential risks, be willing to participate in the research and practice of high-altitude ladder deoxygenation therapy, and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Serious illness: The candidate suffers from severe heart, lung, or circulatory system diseases and cannot withstand the physiological challenges brought by high-altitude stepwise deoxygenation therapy; 2. Pregnant women or participants with severe psychological disorders; 3. Having traveled to or resided in the plateau for a long time.

Design outcomes

Primary

MeasureTime frame
Time to achieve preliminary acclimatization;Safety outcomes (including adverse events, vital signs, and laboratory abnormalities);

Secondary

MeasureTime frame
Incidence rate of acute mountain sickness;Incidence rate of psychological disorders;Proportion of complete, basic, preliminary, and non-acclimatization;Proportion of severe altitude sickness;Proportion of recurrent altitude illness after acclimatization;Total oxygen consumption;

Countries

China

Contacts

Public ContactWang Bowen

General Hospital of Xizang Military Command of the Chinese People's Liberation Army

1491867642@qq.com+86 891 685 8120

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026