Skip to content

Clinical study on intervention of Huoxue Qianyang Decoction on early renal damage in hypertension

Clinical study on intervention of Huoxue Qianyang Decoction on early renal damage in hypertension

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001947
Enrollment
Unknown
Registered
2025-10-15
Start date
2024-12-31
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

hypertension

Interventions

Placebo group:On the basis of lowering blood pressure and protecting renal function RAS system inhibitor is combined with placebo granules
Huoxue Qianyang Granule Group:RAS system inhibitor combined with Huoxue Qianyang Granule on the basis of lowering blood pressure.

Sponsors

Longhua Hospital of Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients meeting the diagnostic criteria for primary hypertension according to the 2024 Chinese Guidelines for Hypertension Diagnosis and Treatment, and receiving at least one type of RAS inhibitor. (2) Meeting the diagnostic criteria for early-stage hypertensive renal impairment. (3) Meeting the diagnostic criteria for the TCM syndrome pattern of "blood stasis with yang hyperactivity". (4) Age 35–80 years. (5) Voluntarily participating and having signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Failure to meet the inclusion criteria. (2) Patients with glaucoma. (3) Patients with dizziness or headache caused by other conditions (e.g., anemia, hyperthyroidism, severe neurosis, cervical spondylosis, tumors, hypotension). (4) Patients with severe primary diseases (cerebrovascular, hepatic, renal, hematopoietic system disorders) or severe cardiac dysfunction, or psychiatric disorders. (5) Pregnant or lactating women, or women planning pregnancy. (6) Patients with congenital heart disease, valvular heart disease, cor pulmonale, cardiomyopathy, pericardial effusion, or pleural effusion confirmed by physical or auxiliary examinations. (7) Patients with secondary hypertension. (8) Patients with refractory hypertension. (9) Patients with allergic constitutions or multiple drug allergies. (10) Patients meeting inclusion criteria but excluded due to non-adherence to protocol-specified medication, unevaluable efficacy, or incomplete data affecting safety/efficacy assessment.

Design outcomes

Secondary

MeasureTime frame
Integrals of TCM syndromes;kidney function;24-hour mean blood pressure(ABP);Urinary Albumin-to-Creatinine Ratio (UACR);cystatin c;Glomerular Filtration Rate (GFR);

Primary

MeasureTime frame
Urinary Microalbumin(MAU);

Countries

China

Contacts

Public ContactWang.Zheng

Longhua Hospital affiliated to Shanghai University of Traditional Chinese Medicine

zwnowayback@126.com+86 021-64385700-13012

Outcome results

None listed

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