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NCT06941935Not yet recruiting

Etiological Classification-guided Individual Intervention in Primary Hypertension

Etiological Classification-guided Individual Intervention in Primary Hypertension: An All-comer Registry Study

Source: ClinicalTrials.gov · Last updated 24 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Eligible participants will first undergo a 1-week home blood pressure diary and 24-hour ambulatory blood pressure assessment. After a confirmed diagnosis of hypertension, etiological subtyping will be performed. Based on the blood pressure evaluation results and etiological classification, the most appropriate antihypertensive medication will be selected. Simultaneously, a personalized lifestyle prescription will be provided according to the patient's individual circumstances. Following medication initiation, participants will continue to monitor their blood pressure through home diaries. Monthly evaluations will be conducted, and if blood pressure fails to reach the target value, medication adjustments will be made based on the blood pressure diary until target levels are achieved. This regimen will be maintained long-term.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
2000 (estimated)
First submitted
13 Apr 2025
Start date
1 Jun 2025
Primary completion date
31 Dec 2030
Lead sponsor
Shanghai 10th People's Hospital
NCT number
NCT06941935

What you commit to

  • Study type: Interventional
  • Planned participants: 2000
  • From 1 Jun 2025 to the primary completion date, 31 Dec 2030
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Secondary hypertension or arrhythmias affecting blood pressure accuracy (e.g., atrial fibrillation).
  • History of stroke or myocardial infarction.

Lab values

  • Comorbidities such as diabetes, chronic kidney disease (eGFR \< 30 mL/min/1.73m²), coronary artery disease, heart failure, or serious valvular heart disease.

Other

  • Pregnancy, breastfeeding, or planning to become pregnant.
  • Life expectancy \< 1 year.
  • Participation in another clinical trial.

Who the study is looking for

  • Age 18-65 years.
  • Diagnosed primary hypertension (systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg).
  • signed informed consent.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Shanghai Tenth People's Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
Department of Cardiology, Shanghai Tenth People's Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.