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A retrospective cohort study on the treatment of primary hypertension with Angong Jiangya Pill based on the real world

A retrospective cohort study on the treatment of primary hypertension with Angong Jiangya Pill based on the real world

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080340
Enrollment
Unknown
Registered
2024-01-26
Start date
2024-02-19
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

primary hypertension

Interventions

Exposure group (Treatment of patients with primary hypertension using Angong Jiangya Pill):NA
Non exposed group (Patients with primary hypertension treated only with conventional Western medicine antihypertensive drugs):NA

Sponsors

The Third Affiliated Hospital of Beijing University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Consistent with the diagnosis of primary hypertension in Western medicine or the diagnosis of liver yang hyperactivity in traditional Chinese medicine vertigo; (2) The patient is = 18 years old, regardless of gender; (3) Patients who visited between January 2018 and December 2022 and have at least one follow-up record; (4) No Angong Jiangya Pill or traditional Chinese patent medicines and simple preparations similar to Angong Jiangya Pill (such as Naoliqing Pill, Qingnao Jiangya Tablet, Niuhuang Jiangya Pill, etc.) was taken at least one month before the observation.

Exclusion criteria

Exclusion criteria: (1) During the observation period, traditional Chinese patent medicines and simple preparations (such as Naoliqing Pill, Qingnao Jiangya Tablet, Niuhuang Jiangya Pill, etc.) with similar effects to Angong Jiangya Pill were taken; (2) Patients with secondary hypertension; (3) Concomitant with severe primary diseases such as heart, liver, and kidney; (4)The case data is incomplete, and the main observation indicators are severely missing.

Design outcomes

Primary

MeasureTime frame
Clinic blood pressure;Symptom score;

Secondary

MeasureTime frame
Dynamic blood pressure;

Countries

China

Contacts

Public ContactTang Qisheng

The Third Affiliated Hospital of Beijing University of Traditional Chinese Medicine

tangqisheng@263.net+86 10 5207 5438

Outcome results

None listed

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