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Real-world study on the efficacy and safety of Bevanolol hydrochloride tablets in the treatment of essential hypertension

Real-world study on the efficacy and safety of Bevanolol hydrochloride tablets in the treatment of essential hypertension

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052370
Enrollment
Unknown
Registered
2021-10-24
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

primary hypertension

Interventions

Sponsors

Qinzhou First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old, male or female; 2. According to the diagnostic criteria of the Chinese guidelines for the prevention and treatment of hypertension (2018 revision), the diagnosis is primary Hypertension; 3. Have taken bevanolol hydrochloride tablets before or plan to take bevanolol hydrochloride tablets; 4. Voluntarily participate and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who have a history of allergies or contraindications to the research drugs and excipients; 2. History of chronic diseases or serious diseases such as liver and kidney; 3. Patients with severe cerebrovascular disease within 6 months before enrollment in this trial; 4. Pregnant and lactating women; 5. The researcher believes that it is not suitable to participate in this researcher.

Design outcomes

Primary

MeasureTime frame
Change of sitting diastolic blood pressure relative to baseline value after administration;

Secondary

MeasureTime frame
Change of sitting systolic blood pressure relative to baseline value after administration;Effective rate of hypotension after medication;Changes in heart rate after medication;

Countries

China

Contacts

Public ContactGeng Dan

Qinzhou First People's Hospital

775410673@qq.com+86 13217771968

Outcome results

None listed

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