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Pathogenesis, Molecular Targets and Intervention Strategies of High-Altitude Heart Disease

Pathogenesis, Molecular Targets and Intervention Strategies of High-Altitude Heart Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116323
Enrollment
Unknown
Registered
2026-01-08
Start date
2026-01-15
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

High-altitude heart disease

Interventions

Transcriptomics cohort: HAHD patients:None
Transcriptomics cohort: Healthy controls at the same altitude:None
Proteomics cohort: HAHD patients:None
Proteomics cohort: Healthy controls at the same altitude:None
Group 1 (High Altitude Heart Disease group): Control group:Intermittent oxygen therapy
Group 1 (High Altitude Heart Disease group): Intervention Group 1 (Intermittent oxygen therapy + calcium antagonist [amlodipine 5 mg qd]):Intermittent oxygen therapy + calcium antagonist (amlodipine 5
Group 1 (High Altitude Heart Disease group): Intervention Group 2:Intermittent oxygen therapy + targeted drug therapy (phosphodiesterase-5 inhibitor, endothelin receptor antagonist)
Group 2 (High Altitude Heart Disease with Right Heart Failure group): Control group (conventional therapy):Oxygen therapy + basic treatment
Group 2 (High Altitude Heart Disease with Right Heart Failure group): Trial group:Conventional therapy + SGLT2i

Sponsors

Xizang Autonomous Region People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Part 1: Individuals meeting the diagnostic criteria for High Altitude Heart Disease (HAHD); a healthy control group at the same altitude was simultaneously established. All participants were recruited from patients admitted to the Department of Cardiology, Tibet Autonomous Region People’s Hospital, with a residence altitude >= 3500 m and continuous residence for >= 6 months. Part 2: 1. Group 1 (High Altitude Heart Disease group): Met the diagnostic criteria for high altitude heart disease without signs of right heart failure; 2. Group 2 (High Altitude Heart Disease with Right Heart Failure group): Met the diagnostic criteria for high altitude heart disease with concomitant right heart failure (right atrial pressure RAP >= 15 mmHg, cardiac index < 2.0 L·min^-1·m^-2)

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Transcriptomic and proteomic data;Event-Free Survival (EFS);Functional Improvement: Improvement in NYHA Functional Class by =1 grade;Exercise Tolerance: Improvement in Six-Minute Walk Distance by =50 meters;

Secondary

MeasureTime frame
Hemodynamic Improvement: Reduction in Right Atrial Pressure, Pulmonary Artery Pressure, and Improvement in Cardiac Index;Biomarkers: Changes in BNP and NT-proBNP Levels;Quality of Life: Minnesota Living with Heart Failure Questionnaire (MLHFQ) Score;Hospitalization Rate;

Countries

China

Contacts

Public ContactKelsang Norbu

Xizang Autonomous Region People's Hospital

kelsangnorbu@hotmail.com+86 135 4901 0066

Outcome results

None listed

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