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Standardized, Intelligent, and Digital Prevention and Control System for Major Cardiopulmonary and Cerebrovascular Diseases on the Plateau Based on Multi-Center Population Cohort Studies

Standardized, Intelligent, and Digital Prevention and Control System for Major Cardiopulmonary and Cerebrovascular Diseases on the Plateau Based on Multi-Center Population Cohort Studies

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122485
Enrollment
Unknown
Registered
2026-04-14
Start date
2026-04-14
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Major cardiovascular, pulmonary, and cerebral diseases in plateau regions

Interventions

Observational group (Risk Assessment Group / Dynamic Adaptation Group (Plateau Period) / Patient Group):None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Risk Assessment Group (Before Entry): (1) Aged 18-60 years; (2) Planning to work or live in high-altitude areas (elevation >= 2,500 meters) within the next 3 months; (3) Sign the informed consent form; 2. Dynamic Adaptation Group (During Highland Period): (1) Having continuously lived in high-altitude areas for no more than 1 year, or after members of the included risk assessment group enter the highlands; (2) Aged 18-75 years; (3) Sign the informed consent form; 3. Patient Group: (1) Clinically diagnosed with major cardiopulmonary or cerebrovascular diseases such as high-altitude pulmonary edema, high-altitude cerebral edema, or high-altitude heart disease; (2) Aged >=18 years; (3) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with severe mental illnesses or cognitive impairments who are unable to cooperate with the research process; 2. Pregnant or breastfeeding women (due to potential risks of certain examinations); 3. Patients with advanced malignant tumors or other end-stage diseases with an expected survival of less than 1 year; 4. Other situations deemed by the researcher as unsuitable for participation in this study (such as long-term alcoholism, drug abuse, etc.).

Design outcomes

Primary

MeasureTime frame
Major cardiopulmonary and cerebrovascular diseases occurrence;Outcomes;History of high altitude Travel and Residence;

Secondary

MeasureTime frame
Disease severity;Demographics(Permanent residence altitude, duration on the altitude, etc.);Vital signs;Medical history;Physical examination;Laboratory test(blood routine, biochemistry, myocardial enzyme spectrum, coagulation function, etc.);Imaging data (e.g., chest X-ray, echocardiography,PFT;Wearable device monitoring data (e.g.,blood oxygen saturation, cerebral oxygen saturation, heart rate, blood pressure, pulmonary artery pressure);Telemedicine records;

Countries

China

Contacts

Public ContactFengming Luo

West China Hospital, Sichuan University

fengmingluo@outlook.com+86 189 8060 1355

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026