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Clinical effectiveness study of traditional Chinese medicine compound preparations in the treatment of hypertension

Clinical comprehensive evaluation of traditional Chinese medicine compound preparations for the treatment of hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075066
Enrollment
Unknown
Registered
2023-08-24
Start date
2023-08-27
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Hypertension

Interventions

Intervention group:According to the dosage requirements of this product
The route of administration for this product is oral
Dosage frequency and dose: 1. Blood pressure level: SBP 140~149 mmHg and/or DBP 90~99 mmHg
Dosage (intervention phase): 1 capsule in the morning and evening
Duration of use (intervention phase): 7±5 days
Dosage (after blood pressure stabilization, dose reduction phase): 1 capsule every 5 days
Duration of use (dose reduction phase): 14 days. 2. Blood pressure level: SBP 150~159 mmHg and/or DBP 90~99/=99 mmHg
Dosage (intervention phase): 2 capsules in the morning and evening
Duration of use (intervention phase):10±5 days
Dosage (after blood pressure stabilization, dose reduction phase):1 capsule every3days
Durationofuse(dosereductionphase) :14days.

Sponsors

Lanzhou University First Hospital; School of Basic Medical Sciences, Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age: 18 years old and above; (2) Fully understand and voluntarily sign the informed consent form; (3) Patients diagnosed with primary hypertension and mild hypertension, including ? newly diagnosed hypertensive patients who have not received any antihypertensive medications, or ? patients diagnosed with hypertension who have a history of taking antihypertensive medications. Must meet all the above criteria to be included.

Exclusion criteria

Exclusion criteria: (1) Patients with allergic reactions to this medication; (2) Liver dysfunction; (3) Impaired liver function; (4) Pregnant and lactating women; (5) Participated in other clinical trials within the past 3 months; (6) Situations deemed unsuitable for participation in this study by the researchers. Any of the above criteria, do not include.

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure (SBP);Diastolic blood pressure (DBP);

Secondary

MeasureTime frame
Pulse and heart rate;Adverse events;Heart rate;

Countries

China

Contacts

Public ContactJunqiang Niu; Wenru Shang

Lanzhou University First Hospital; Lanzhou University

shangwr@lzu.edu.cn+86 199 2187 4252

Outcome results

None listed

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