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Effect of oral terazosin hydrochloride tablets or exercise intervention on the degree of arteriosclerosis in middle-aged and elderly people

Effect of oral terazosin hydrochloride tablets or exercise intervention on the degree of arteriosclerosis in middle-aged and elderly people

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300079001
Enrollment
Unknown
Registered
2023-12-22
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Atherosclerosis

Interventions

Drug intervention group:oral terazosin hydrochloride tablets(0.5mg once a night)
Exercise intervention group:150 minutes of moderate exercise per week

Sponsors

Xijing Hospital, the First Affiliated Hospital of Air Force Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Over 40 years old, under 75 years old; ? Abnormal increase of baPWV, exceeding the normal reference value (1400cm/s) ? Control stable coronary heart disease, hypertension, no obvious sequelae of past stroke patients. ? Normal or mildly abnormal liver and kidney function ? no blood system diseases; ? Meets the following criteria: a. Self-care or basically self-care; b. Cognitive function is basically normal ? Sign informed consent.

Exclusion criteria

Exclusion criteria: ? People who have taken terazosin in the past three months or are allergic to it; ? Have taken Tamsulosin sustained-release capsules in the past three months; ? Patients hospitalized in the past 3 months due to major cardiovascular and cerebrovascular events, including myocardial infarction, angina pectoris, stroke, and arterial revascularization; ? Patients with heart failure and heart function below Grade II; ? Patients with malignant tumors; ? Can not cooperate with treatment and follow-up; ?Participating in other clinical trials; ? Inability to tolerate investigational drugs; ? Pregnant or lactating women; ? Those that researchers believe should not be included.

Design outcomes

Primary

MeasureTime frame
Brachial-ankle pulse wave velocity;

Secondary

MeasureTime frame
Carotid intima-media thickness;Circulating inflammatory factor;blood lipid;

Countries

China

Contacts

Public ContactWang Xiaoming

Xijing Hospital, the First Affiliated Hospital of Air Force Military Medical University

xmwang@fmmu.edu.cn+1 819 202 8999

Outcome results

None listed

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