Key Diagnostic & Therapeutic Technologies for Severe Acute High Altitude Disease (SAHAD): Integration and Application

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorTibet Autonomous Region People's Hospital

About this trial

This study aims to establish a key technical system for the diagnosis and treatment of severe acute mountain sickness based on real-world clinical data in Xizang, develop standardized diagnosis and treatment protocols and an intelligent early warning model, validate its efficacy through multicenter studies, and innovate diagnostic and therapeutic technologies. It will achieve early identification, precise diagnosis, standardized treatment, and intelligent warning of severe acute mountain sickness, comprehensively improving its prevention, control and treatment success rate.

Eligibility criteria

Qualifiers

Meeting the diagnostic criteria for severe acute mountain sickness (including high-altitude pulmonary edema [HAPE] and high-altitude cerebral edema [HACE]).

Aged 18 to 75 years.

Rapid ascent to an altitude above 2500 m within 72 hours prior to onset.

Disqualifiers

History of severe cardiopulmonary diseases.

Pregnant women, patients with psychiatric disorders, inability to cooperate with treatment or follow-up, and patients with an expected survival of less than 6 months.

Patients with malignant tumors, severe hepatic or renal insufficiency, or immune system diseases requiring immunosuppressive therapy.

Trial design

Treatments tested in this trial

  • Multicenter study of HAPE:CPAP or BiPAP Group
  • Multicenter study of HAPE group:NO Group
  • Protocol for Proteomics and Peptidomics Study of HAPE:Case Group

Treatment groups

3,035 Participants
are divided into 13 treatment groups

13

Treatment groups

See each treatment group below.