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Study on the standardization scheme of traditional Chinese medicine treatment of grade 1 hypertension based on Kugan granule

Study on the standardization scheme of traditional Chinese medicine treatment of grade 1 hypertension based on Kugan granule

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087475
Enrollment
Unknown
Registered
2024-07-29
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

Essential hypertension

Interventions

Control group:Valsartan Capsules
Test group:Kugan granules

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Province Hospital of Chinese Medicine)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Aged between 18 and 85, any gender. (2) Diagnosed with stage 1 hypertension according to Western medicine standards. (3) Display symptoms of excessive liver fire or phlegm-dampness in Traditional Chinese Medicine. (4) Have no history of previous antihypertensive medication use, or have discontinued use for over 2 weeks and meet the above diagnostic criteria. (5) Understand the research content, willingly participate in this study, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Secondary hypertension or hypertensive emergency. (2) Pregnant and lactating women. (3) Combined with severe target organ damage, including cerebral hemorrhage, cerebral infarction, myocardial infarction, etc. (4) Patients with severe liver and kidney function impairment or combined with heart, lung and other organ failure. (5) Those who have clear contraindications and allergies to the test drugs (components of traditional Chinese medicine granules, ARB). (6) Those with severe hearing, language, communication and cognitive dysfunction and unable to complete the scale; (7) Currently participating in other drug clinical trials.

Design outcomes

Primary

MeasureTime frame
Office Blood Pressure;Ambulatory blood pressure;Main symptoms;

Secondary

MeasureTime frame
Four items of blood lipid tests;Fasting plasma glucose;Glycated serum proteins;Fasting insulin;Uric acid;

Countries

China

Contacts

Public ContactShi Wang

Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Province Hospital of Chinese Medicine)

suewang08@126.com+86 180 0515 8100

Outcome results

None listed

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