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Fixed-dose Combination for Antihypertensive Therapy in the Community Healthcare

Fixed-dose Combination for Antihypertensive Therapy in the Community Healthcare

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000320
Enrollment
Unknown
Registered
2008-10-16
Start date
2008-09-25
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

hypertension

Interventions

Group B:FUFANGJIANGYAPIAN 1 TABLET, 1 TABLET TID PO
Group A:FUFANGJIANGYAPIAN 1 TABLET, 1 TABLET TID PO

Sponsors

Fuwai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Primary hypertension, SBP>=140 mmHg and/or DBP>=90mmHg, SBP65years; current smoker; overweight or obesity; abnormal blood lipid level; family CVD history; controlled type II diabetes; IMT>=0.9mm; stroke history; identified TIA history; MI history; stable angina; coronary revascularization history; cardiac insufficiency; peripheric vessel disease; chronic renal disease.

Exclusion criteria

Exclusion criteria: Secondary hypertension, within 3 month of acute CVD event, UAP, severe liver or renal diseases, type I diabetes or uncontrolled type II diabetes, active gastrointestinal ulcer, gout, established histroy of depression, malignancy, pregnant women or women using contraceptive, HIV positive, mental disorder or alcohol/ drug abuse in the last 5 years, or uncontrolled mental illness, concern about participant participation, currently participate in other clinical trials, allergies to study medications, contradictions of study medications,not be suitable for the trial based on the physician's knowledge

Design outcomes

Primary

MeasureTime frame
cost-efficacy;CVD event;Accident of pneumonia, fracture;

Secondary

MeasureTime frame
complaince;blood pressure;

Countries

China

Contacts

Public ContactZengwu Wang
catchbj@126.com+86 010 88398070

Outcome results

None listed

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