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Luohe Hypertension and Panvascular Disease Cohort Study

Luohe Hypertension and Panvascular Disease Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127268
Enrollment
Unknown
Registered
2026-06-28
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Primary Diseases: Hypertension, Pan-vascular Diseases, Hypertensive Target Organ Damage. Related Adverse Events and Comorbidities: Myocardial infarction, Stroke, Heart failure, Coronary artery ischemic lesions, Peripheral arterial disease, Carotid/renal artery stenosis, Aortic diseases, End-stage renal disease, Cardiac death, Arrhythmia, Cardiogenic shock, Cardiometabolic abnormalities, Sleep and

Interventions

Luohe Hypertension and Panvascular Disease Cohort Study:None

Sponsors

Luohe Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 years or older. 2.Receiving hospitalization, consultation, follow-up or management at Luohe Central Hospital or its affiliated network hospitals, with complete access to major clinical and key diagnostic data. 3.Meeting the diagnostic criteria for hypertension. 4.Having at least one pan-vascular assessment record at baseline, such as baPWV/ABI, carotid ultrasound, renal artery imaging, cranial imaging, electrocardiogram, echocardiogram or other vascular/target organ examinations. Completion of baPWV/ABI is recommended; reasons for failure will be documented, which shall not be a sole exclusion factor. 5.The participant, legal representative or regular caregiver is willing and able to complete 30-year annual follow-up via telephone, outpatient visit or medical records, and provides valid contact information for themselves and at least one relative.

Exclusion criteria

Exclusion criteria: 1.Critically unstable acute conditions judged by the research team to preclude baseline assessment or follow-up. 2.Acute unstable phase of myocardial infarction, acute coronary syndrome, acute stroke or acute decompensated heart failure. 3.Active malignancy, end-stage organ failure or other severe non-cardiovascular diseases with limited life expectancy (< 1 year) or inability to complete follow-up. 4.Severe mental disorders, disturbance of consciousness or cognitive impairment unable to cooperate with questionnaires and follow-up, with no eligible legal representative or caregiver available. 5.No valid contact information or confirmed inability to receive long-term follow-up. 6.Pregnant women (confirmed or clinically suspected pregnancy). 7.Severe missing key clinical or pan-vascular assessment data that prevents baseline risk evaluation and long-term outcome judgment.

Design outcomes

Primary

MeasureTime frame
First MACCE occurring after baseline. MACCE consists of all-cause death (cardiac death will be identified and documented), non-fatal myocardial infarction, non-fatal stroke, hospitalization for heart;

Secondary

MeasureTime frame
Cardiac death.;

Countries

China

Contacts

Public ContactWang Haoran

Luohe Central Hospital

18339561986@163.com+86 395 3330559

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026