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Observational Study on Optimizing Treatment for Patients with Resistant Hypertension

Observational Study on Optimizing Treatment for Patients with Resistant Hypertension

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091139
Enrollment
Unknown
Registered
2024-10-22
Start date
2024-10-31
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

resistant hypertension

Interventions

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) Despite the use of three antihypertensive drugs at tolerable and sufficient doses (including a thiazide diuretic, with the other two being any of the five major classes of antihypertensive drugs recommended by the "2018 Chinese Guidelines for the Prevention and Treatment of Hypertension" [calcium channel blockers (CCBs), angiotensin-converting enzyme inhibitors (ACEIs), angiotensin II receptor blockers (ARBs), diuretics, and beta-blockers], this study will also consider other drug types such as aldosterone receptor antagonists and alpha-blockers), blood pressure remains above the target level (office blood pressure measured on three different occasions shows systolic blood pressure =140 mmHg and/or diastolic blood pressure =90 mmHg, with a 24-hour average blood pressure >130/80 mmHg); (2) Age between 18 and 79 years; (3) Signed informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with a confirmed diagnosis of secondary hypertension; (2) Patients with severe heart failure (New York Heart Association [NYHA] Class 3-4); (3) Patients with acute myocardial infarction; (4) Patients in the acute phase of stroke; (5) Patients with severe liver dysfunction (ALT > 3 times the upper limit of normal and BIL > 2 times the upper limit of normal); (6) Patients with severe renal failure (eGFR < 30 mL/1.73 m²); (7) Patients with congenital heart disease; (8) Patients with malignant tumors or severe infections; (9) Pregnant or breastfeeding women; (10) Patients participating in other clinical studies; (11) Patients unable to provide informed consent; (12) Patients deemed unsuitable for enrollment or unable to complete follow-up according to the judgment of the physician.

Design outcomes

Primary

MeasureTime frame
SBP;DBP;

Secondary

MeasureTime frame
BP out of office ;

Countries

China

Contacts

Public ContactYuqing Zhang

Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

yqzhang9988@163.com+86 136 0132 9207

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026