Skip to content

A randomized controlled study of integrated traditional Chinese and western medicine prevention and treatment plan for borderline hypertension

A randomized controlled trial of combined pathological evidence and lifestyle intervention for the treatment of phlegm-damp internal obstruction type borderline hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006379
Enrollment
Unknown
Registered
2022-07-26
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Borderline Hypertension

Interventions

Experimental group:Ershu Tianma Granules 1 dose,2/d
Control group:Ershu Tianma placebo Granules 1 dose,2/d

Sponsors

Eye Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ?No antihypertensive medication in the last 4 weeks and three consecutive upper limb brachial artery sitting blood pressure measurements on non-same day within 1 week, systolic blood pressure (SBP) 120-139 mmHg and/or diastolic blood pressure (DBP) 80-89 mmHg. ?Age 18-65 years old, gender not limited. ?Meet the diagnostic criteria of phlegm-dampness internal obstruction evidence. ?Voluntary participation and cooperation with the investigator by signing the written informed consent.

Exclusion criteria

Exclusion criteria: ?People with definite primary and secondary hypertension. ?Participating in other clinical researchers. ?People with borderline hypertension who are taking western antihypertensive drugs. ?People with acute coronary syndrome, acute attack of chronic heart failure, malignant arrhythmia, heart valve disease, cardiomyopathy and other serious cardiovascular diseases. ?People with acute or severe cerebrovascular diseases such as cerebral hemorrhage, subarachnoid hemorrhage, cerebral infarction and transient ischemic attack. ?People with severe liver or kidney dysfunction and conditions judged by the investigator to be inappropriate for enrollment. ?Pregnant and lactating women. ?Allergic or allergic to multiple drugs.

Design outcomes

Primary

MeasureTime frame
Consulting room blood pressure;

Secondary

MeasureTime frame
Body mass index;Waist Circumference;Homocysteine;Home Self-Test Blood Pressure;Uric Acid;Chinese medicine evidence score;Fasting blood sugar;Ambulatory blood pressure mean blood pressure values;Ambulatory blood pressure load values and circadian rhythms;C-reactive protein;Serum lipid level;Quality of life;

Countries

China

Contacts

Public ContactYao Kuiwu

Eye Hospital of China Academy of Chinese Medical Sciences

yaokuiwu@126.com18610366611

Outcome results

None listed

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